Filed pursuant to General Instruction II.L of Form F-10;
File No. 333-161786
PROSPECTUS
SUPPLEMENT
(To Short
Form Base Shelf Prospectus dated September 16, 2009)
No securities regulatory authority
has expressed an opinion about these securities and it is an offence to claim
otherwise
. This prospectus supplement, together with the accompanying
short form base shelf prospectus dated September 16, 2009 to which it relates,
as amended or supplemented, and each document deemed to be incorporated by
reference into this prospectus supplement and the short form base shelf
prospectus, constitutes a public offering of these securities only in those
jurisdictions where they may be lawfully offered for sale and therein only by
persons permitted to sell such securities. See "Plan of
Distribution".
Information has been incorporated by
reference in this prospectus supplement and the accompanying short form base
shelf prospectus from documents filed with the Ontario Securities
Commission
. Copies of the documents incorporated by reference in this
prospectus supplement and the short form base shelf prospectus may be obtained
on request without charge from Vice-President, Finance and Administration of YM
BioSciences Inc. at Suite 400, Building 11, 5045 Orbitor Drive, Mississauga,
Ontario, Canada L4W 4Y4, Telephone: (905) 629-9761 and are also available
electronically at www.sedar.com.
Up
to 7,750,000 Common Shares
We are
hereby qualifying for distribution up to 7,750,000 common shares of YM
BioSciences Inc. We have entered into a controlled equity offering sales
agreement dated as of April 23, 2010 (the “sales agreement”) with Cantor
Fitzgerald & Co. (“CF&Co”) relating to common shares offered by this
prospectus supplement and the accompanying short form base shelf prospectus
dated September 16, 2009. In accordance with the sales agreement, and
except as noted below, we may distribute up to 7,750,000 common shares through
CF&Co, as our agent or as principal for the distribution of the common
shares. See “Plan of Distribution” beginning on page S-14 of this
prospectus supplement for more information regarding these
arrangements.
Our
business and an investment in our common shares involve significant risks. See
“Risk Factors”
beginning on page S-
9
of this prospectus
supplement and on page 7 of the accompanying prospectus
.
NEITHER
THE UNITED STATES SECURITIES AND EXCHANGE COMMISSION NOR ANY STATE SECURITIES
REGULATOR HAS APPROVED OR DISAPPROVED OF THESE SECURITIES OR DETERMINED IF THIS
PROSPECTUS SUPPLEMENT OR THE ACCOMPANYING PROSPECTUS IS TRUTHFUL OR COMPLETE.
ANY REPRESENTATION TO THE CONTRARY IS A CRIMINAL OFFENCE.
We
are permitted, under a multi-jurisdictional disclosure system adopted by the
United States, to prepare this prospectus supplement and the accompanying short
form base shelf prospectus in accordance with Canadian disclosure requirements,
which are different from those of the United States. We prepare our financial
statements, which are incorporated by reference in this prospectus supplement
and the accompanying prospectus, in accordance with Canadian generally accepted
accounting principles, and they are subject to Canadian auditing and auditor
independence standards. Our financial statements may not be comparable to the
financial statements of US companies. Additionally, financial statements of
Cytopia Limited
(now YM BioSciences Australia Pty
Ltd.)
contained in our business acquisition report dated February 12,
2010 and incorporated by reference in this prospectus supplement and the
accompanying prospectus were prepared in accordance with Australian accounting
standards which include Australian equivalents to International Financial
Reporting Standards and were subject to Australian auditing and auditor
independence standards and such financial statements may not be comparable to
the financial statements of Canadian companies or US companies.
Purchasing
our common shares may subject you to tax consequences both in the United States
and Canada. This prospectus supplement and the accompanying prospectus may not
describe these tax consequences fully. You should read the tax discussion in
this prospectus supplement and the accompanying prospectus fully and consult
with your own tax advisers.
Your
ability to enforce civil liabilities under United States federal securities laws
may be affected adversely because we are continued under the laws of Nova
Scotia, Canada, a majority of our directors are not US residents and a majority
of our officers and certain of the experts named in this prospectus supplement
and the accompanying prospectus are residents of Canada and a substantial
portion of our assets are located outside the United States.
CF&Co
will receive a cash fee equal up to but not exceeding 5.0% of the first
aggregate gross proceeds of US$5 million and thereafter 3% of the gross proceeds
realized from the sale of our common shares for services rendered in connection
with the offering. See “Plan of Distribution”.
We
estimate the total expenses of this offering, excluding CF&Co’s fee, will be
approximately US$175,000.
No
underwriter or dealer involved in this offering, no affiliate of such an
underwriter or dealer, and no person acting jointly or in concert with such an
underwriter or dealer has over-allotted, or will over-allot, common shares with
the offering or effect any other transactions that we intended to stabilize or
maintain the market price of the common shares.
Our
common shares are listed on the Toronto Stock Exchange under the symbol “YM” and
on the NYSE Amex under the symbol “YMI”. On April 23, 2010, the last
reported sale price of our common shares on the TSX was C$1.48 per share and
US$1.47 per share on the NYSE Amex. The TSX has conditionally
approved the listing of the common shares offered by this prospectus
supplement. Listing is subject to us fulfilling all of the
requirements of the TSX within one business day of the date
hereof. The NYSE Amex has authorized, upon official notice of
issuance, the listing of the common shares offered hereunder.
Sales of
common shares, if any, under this prospectus supplement and the accompanying
prospectus may be made in transactions that are deemed to be “at-the-market
distributions” as defined in National Instrument 44-102 – Shelf Distributions
(“NI 44-102”), including sales made directly on the, NYSE Amex or other existing
trading markets for the common shares in the United States. The
common shares will be distributed at market prices prevailing at the time of the
sale of such common shares. As a result, prices may vary as between
purchasers and during the period of distribution.
TABLE
OF CONTENTS
Prospectus
Supplement
IMPORTANT
NOTICE
|
ii
|
ABOUT
THIS PROSPECTUS SUPPLEMENT
|
S-1
|
SPECIAL
NOTE REGARDING FORWARD-LOOKING STATEMENTS
|
S-2
|
DOCUMENTS
INCORPORATED BY REFERENCE
|
S-4
|
RECENT
DEVELOPMENTS
|
S-7
|
RISK
FACTORS
|
S-8
|
EXCHANGE
RATE INFORMATION
|
S-12
|
CONSOLIDATED
CAPITALIZATION
|
S-12
|
TRADING
PRICE AND VOLUME
|
S-12
|
PRIOR
SALES
|
S-12
|
USE
OF PROCEEDS
|
S-13
|
DETAILS
OF THE OFFERING
|
S-13
|
PLAN
OF DISTRIBUTION
|
S-14
|
MATERIAL
UNITED STATES FEDERAL INCOME TAX
CONSIDERATIONS
|
S-15
|
WHERE
YOU CAN FIND MORE INFORMATION
|
S-22
|
ENFORCEMENT
OF CIVIL LIABILITIES
|
S-22
|
LEGAL
MATTERS
|
S-23
|
Prospectus
dated September 16, 2009
EXCHANGE
RATES
|
1
|
PRESENTATION
OF FINANCIAL INFORMATION
|
2
|
DOCUMENTS
INCORPORATED BY REFERENCE.
|
2
|
ADDITIONAL
INFORMATION
|
3
|
ENFORCEABILITY
OF CIVIL LIABILITIES
|
4
|
SPECIAL
NOTE REGARDING FORWARD-LOOKING STATEMENTS
|
4
|
RISK
FACTORS
|
7
|
PROBABLE
ACQUISITIONS OR OTHER MATERIAL TRANSACTIONS
|
17
|
USE
OF PROCEEDS
|
17
|
DESCRIPTION
OF SHARE CAPITAL, COMMON SHARES AND RELATED INFORMATION
|
17
|
DESCRIPTION
OF WARRANTS
|
18
|
DESCRIPTION
OF UNITS
|
19
|
PLAN
OF DISTRIBUTION
|
19
|
MATERIAL
INCOME TAX CONSIDERATIONS
|
21
|
AUDITORS
|
20
|
LEGAL
MATTERS
|
20
|
TRANSFER
AGENT AND REGISTRAR
|
21
|
DOCUMENTS
FILED AS PART OF THE REGISTRATION STATEMENT
|
21
|
IMPORTANT
NOTICE
This
document is in two parts. The first part is this prospectus supplement, which
describes the specific terms of the securities we are offering and the method of
distribution of those securities and also supplements and updates information
regarding YM BioSciences Inc. contained in the accompanying short form base
shelf prospectus. The second part, the accompanying short form base shelf
prospectus, gives more general information about securities we may offer from
time to time, some of which may not apply to the offering. Both documents
contain important information you should consider when making your investment
decision. This prospectus supplement may add, update or change information
contained in the accompanying prospectus. Before investing, you
should carefully read both this prospectus supplement and the accompanying
prospectus together with the additional information about YM BioSciences Inc. to
which we refer you in the sections of this prospectus supplement entitled
“Documents Incorporated By Reference” and “Where You Can Find More
Information”.
You
should rely only on information contained in this prospectus supplement, the
accompanying prospectus and the documents we incorporate by reference in this
prospectus supplement and the accompanying prospectus. If information
in this prospectus supplement is inconsistent with the accompanying prospectus
or the information incorporated by reference, you should rely on this prospectus
supplement. We have not authorized anyone to provide you with information that
is different. If anyone provides you with any different or inconsistent
information, you should not rely on it. We are offering the common shares only
in jurisdictions where such offers are permitted by law. The information
contained in this prospectus supplement and the accompanying prospectus is
accurate only as of their respective dates, regardless of the time of delivery
of this prospectus supplement and the accompanying prospectus and you should not
assume otherwise.
ABOUT
THIS PROSPECTUS SUPPLEMENT
This
prospectus supplement and the accompanying prospectus are part of a “shelf”
registration statement on Form F-10 that we have filed with the SEC. The shelf
registration statement was declared effective by the SEC on September 17, 2009.
This prospectus supplement does not contain all of the information contained in
the registration statement, certain parts of which are omitted in accordance
with the rules and regulations of the SEC. You should refer to the registration
statement and the exhibits to the registration statement for further information
with respect to us and our securities.
In this
prospectus supplement, unless stated otherwise or the context requires, all
dollar amounts are expressed in US dollars. All references to “$” or
“US$” are to the lawful currency of the United States and all references to “C$”
are to the lawful currency of Canada. In this prospectus supplement,
where applicable, and unless otherwise indicated, amounts are converted from
United States dollars to Canadian dollars and vice versa by applying the noon
rate of exchange of the Bank of Canada on April 23, 2010. See
“Exchange Rate Information”.
Some of
the information contained or incorporated by reference in this prospectus
supplement and the accompanying prospectus concerning economic and industry
trends is based upon or derived from information provided by industry sources.
We believe that such information is accurate and that the sources from which it
has been obtained are reliable. However, we cannot guarantee the accuracy of
such information and we have not independently verified the assumptions upon
which projections of future trends are based.
In this
prospectus supplement unless the context requires otherwise, “YM”, “we”,” us”
and “our” refer to YM BioSciences Inc. and its subsidiaries through which it
operates.
We
prepare our financial statements in accordance with Canadian generally accepted
accounting principles (“Canadian GAAP”), which differ from United States
generally accepted accounting principles (“US GAAP”). Therefore, our
consolidated financial statements incorporated by reference in this prospectus
supplement and in the accompanying prospectus and in the documents incorporated
by reference in this prospectus supplement and in the accompanying prospectus
may not be comparable to consolidated financial statements prepared in
accordance with US GAAP. You should refer to Note 16 of our consolidated
financial statements for the fiscal year ended June 30, 2009 for a discussion of
the principal differences between our financial results determined under
Canadian GAAP and under US GAAP. For our unaudited consolidated financial
statements as at and for each of the three months ended September 30, 2009 and
the three and six months ended December 31, 2009, you should refer to our
reconciliation of our consolidated financial statements as at and for each of
the three months ended September 30, 2009 and the three and six months ended
December 31, 2009 to US GAAP, each of which is incorporated into this prospectus
supplement by reference. See “Documents Incorporated by Reference”.
Additionally, financial statements of Cytopia Limited
(now YM BioSciences Australia Pty Ltd.)
contained
in our business acquisition report dated February 12, 2010 and incorporated by
reference in this prospectus supplement and the accompanying prospectus were
prepared in accordance with Australian accounting standards which include
Australian equivalents to International Financial Reporting Standards (AIFRS)
and were subject to Australian auditing and auditor independence standards and
such financial statements may not be comparable to the financial statements of
Canadian companies or US companies. You should refer to Notes 28 and 29 of the
consolidated balance sheets of Cytopia Limited
(now YM BioSciences Australia Pty Ltd.)
as at
June 30, 2009 and 2008 and the related statements of income, changes in equity
and cash flows for each of the years then ended for a discussion of the
principal differences between financial results determined under (i) Canadian
GAAP and AIFRS; and (ii) US GAAP and AIFRS. For the unaudited interim financial
statements of Cytopia Limited
(now YM BioSciences
Australia Pty Ltd.)
as at and for each of the six months ended December
31, 2009 and 2008, you should refer to Notes 9 and 10 of such financial
statements for a discussion of the principal differences between financial
results determined under (i) Canadian GAAP and AIFRS; and (ii) US GAAP and
AIFRS.
This
prospectus supplement is deemed to be incorporated by reference into the
accompanying short form base shelf prospectus solely for the purposes of the
offering. Other documents are also incorporated or deemed to be incorporated by
reference into this prospectus supplement and into the accompanying short form
base shelf prospectus. See “Documents Incorporated by Reference”.
SPECIAL
NOTE REGARDING FORWARD-LOOKING STATEMENTS
This
prospectus supplement and the accompanying prospectus, including any documents
incorporated by reference, contain “forward-looking statements” within the
meaning of the United States federal securities laws. The words
“may,” “believe,” “will,” “anticipate,” “expect,” “estimate,” “project,”
“future,” and other expressions that are predictions of or indicate future
events and trends and that do not relate to historical matters identify
forward-looking statements. The forward-looking statements in this
prospectus supplement and the accompanying prospectus, including any documents
incorporated by reference, include, among others, statements with respect
to:
|
·
|
our
expected expenditure and accumulated deficit
levels;
|
|
·
|
our
intentions with respect to acquiring or investing in production
facilities;
|
|
·
|
our
ability to obtain sufficient supplies of our
products;
|
|
·
|
our
ability to identify licensable products or research suitable for licensing
and commercialization;
|
|
·
|
the
locations of our clinical trials;
|
|
·
|
our
intention to license products from multiple
jurisdictions;
|
|
·
|
our
ability to obtain necessary funding on favourable terms or at
all;
|
|
·
|
our
potential sources of funding;
|
|
·
|
our
drug development plans;
|
|
·
|
our
ability to obtain licenses on commercially reasonable
terms;
|
|
·
|
the
effect of third party patents on our commercial
activities;
|
|
·
|
our
intentions with respect to developing manufacturing, marketing or
distribution programs;
|
|
·
|
our
expectations with respect to the views toward our products held by
potential partners;
|
|
·
|
our
plans for generating revenue;
|
|
·
|
our
plans for increasing expenditures for the development of certain
products;
|
|
·
|
our
strategy for protecting our intellectual
property;
|
|
·
|
the
sufficiency of our financial resources to support our activities and our
prospective pivotal trials; and
|
|
·
|
our
plans for future clinical trials and for seeking clinical
clearance.
|
Reliance
should not be placed on forward-looking statements, as they involve known and
unknown risks, uncertainties and other factors that may cause the actual results
to differ materially from the anticipated future results expressed or implied by
such forward-looking statements. Factors that could cause actual
results to differ materially from those set forward in the forward-looking
statements include, but are not limited to:
|
·
|
our
ability to obtain, on satisfactory terms or at all, the capital required
for research, operations and
marketing;
|
|
·
|
general
economic, business and market
conditions;
|
|
·
|
our
ability to successfully and timely complete clinical
studies;
|
|
·
|
product
development delays and other uncertainties related to new product
development;
|
|
·
|
our
ability to attract and retain business partners and key
personnel;
|
|
·
|
the
risk of our inability to profitably commercialize our
products;
|
|
·
|
the
extent of any future losses;
|
|
·
|
the
risk of our inability to establish or manage manufacturing, development or
marketing collaborations;
|
|
·
|
the
risk of delay of, or failure to obtain, necessary regulatory approvals
and, ultimately, product launches;
|
|
·
|
dependence
on third parties for successful commercialization of our
products;
|
|
·
|
inability
to obtain quantities of development product in sufficient quantity or at
standards acceptable to health regulatory authorities to complete clinical
trials or to meet commercial
demand;
|
|
·
|
the
risk of the termination or conversion to non-exclusive licenses or our
inability to enforce our rights under our
licenses;
|
|
·
|
our
ability to obtain patent protection and protect our intellectual property
rights;
|
|
·
|
commercialization
limitations imposed by intellectual property rights owned or controlled by
third parties
|
|
·
|
uncertainty
related to intellectual property liability rights and liability claims
asserted against us;
|
|
·
|
the
uncertainty of recovery of advances to
subsidiaries;
|
|
·
|
the
impact of competitive products and
pricing;
|
|
·
|
future
levels of government funding; and
|
|
·
|
additional
risks and uncertainties, many of which are beyond our control, referred to
elsewhere in this prospectus supplement and the accompanying
prospectus.
|
Except as
required by law, we undertake no obligation to publicly update any
forward-looking statements, whether as a result of new information, future
events or otherwise.
DOCUMENTS
INCORPORATED BY REFERENCE
We are
incorporating by reference in this prospectus supplement certain information
contained in documents filed by us with securities regulatory authorities in
Canada. This means that we are disclosing important information to you by
referring you to those documents. The information incorporated by reference is
deemed to be part of this prospectus supplement, except for any information
superseded by information contained directly in this prospectus supplement or in
any other subsequently filed document which also is or is deemed to be
incorporated by reference herein.
You may
obtain copies of the documents incorporated by reference in this prospectus
supplement on request without charge from our Vice-President, Finance and
Administration at Suite 400, Building 11, 5045 Orbitor Drive, Mississauga,
Ontario, Canada, L4W 4Y4, Telephone: (905) 629-9761, as well as through the
sources described below under “Where You Can Find More
Information”.
The
following documents are specifically incorporated by reference in and form an
integral part of the accompanying base shelf prospectus and this prospectus
supplement:
|
(i)
|
our
annual report filed on the SEC Form 20-F for the year ended June 30, 2009,
as subsequently amended on Form 20-F/A, as filed on
SEDAR;
|
|
(ii)
|
our
audited consolidated balance sheets as at June 30, 2009 and 2008 and the
related consolidated statements of operations and comprehensive loss and
deficit cash flows for each of the years ended June 30, 2009, 2008 and
2007, including the notes thereto and the auditors’ report
thereon;
|
|
(iii)
|
management’s
discussion and analysis of our financial condition and results of
operations for the year ended June 30,
2009;
|
|
(iv)
|
our
management information circular dated October 9, 2009 in respect of our
annual general meeting of shareholders held on November 19,
2009;
|
|
(v)
|
our
material change report dated October 9, 2009 regarding the proposed merger
with Cytopia Limited
(now YM BioSciences Australia Pty Ltd
.
);
|
|
(vi)
|
our
unaudited comparative interim consolidated financial statements as at and
for the three and six months ended December 31, 2009, including the notes
thereto;
|
|
(vii)
|
management’s
discussion and analysis of our financial condition and results of
operations for the three and six months ended December 31,
2009;
|
|
(viii)
|
supplemental
information on Canadian and United States Generally Accepted Accounting
Principles in respect of our unaudited comparative interim consolidated
financial statements as at and for the six months ended December 31, 2009
and 2008;
|
|
(ix)
|
our
material change report dated February 3, 2010 regarding the completion of
the merger of Cytopia Limited
(now YM
BioSciences Australia Pty Ltd.)
into
us;
|
|
(x)
|
our
business acquisition report dated February 12, 2010 in respect of our
acquisition of Cytopia Limited
(now YM
BioSciences Australia Pty
Ltd.)
;
|
|
(xi)
|
our
material change report dated March 2, 2010 regarding a civil claim against
the licensor of nimotuzumab; and
|
|
(xii)
|
our
material change report dated March 19, 2010 regarding the completion by us
of a $17.5 million financing on March 10,
2010.
|
All
material change reports (excluding confidential material change reports) and
unaudited interim consolidated financial statements of our company (and
management’s discussion and analysis relating thereto) filed by us with the
securities regulatory authorities in Canada after the date of this prospectus
supplement and prior to the termination of the offering will be deemed to be
incorporated by reference in this prospectus supplement.
When new
documents of the type referred to in the paragraphs above are filed by us with,
and where required accepted, by the securities regulatory authorities in Canada
during the currency of this prospectus supplement, such documents will be deemed
to be incorporated by reference in this prospectus supplement and the previous
documents of the type referred to in the paragraphs above and all material
change reports, unaudited interim consolidated financial statements (and
management’s discussion and analysis relating thereto) and certain prospectus
supplements filed by us with the securities regulatory authorities in Canada
before the commencement of our financial year in which the new documents are
filed will no longer be deemed to be incorporated by reference in this
prospectus supplement. Specifically, (i) our annual report filed on
the SEC Form 20-F for the year ended June 30, 2008, dated September 22, 2008;
(ii) our audited consolidated balance sheets as at June 30, 2008 and 2007 and
the related consolidated statements of operations and comprehensive loss and
deficit cash flows for each of the years ended June 30, 2008, 2007 and 2006,
including the notes thereto and the auditors’ report thereon; (iii) management’s
discussion and analysis of our financial condition and results of operations for
the year ended June 30, 2008; (iv) the management information circular for the
annual and special meeting of shareholders held on November 20, 2008, as filed
on October 30, 2008; (v) our unaudited comparative interim consolidated
financial statements as at and for the three and nine months ended March 31,
2009, including the notes thereto; and (vi) the management’s discussion and
analysis of our financial condition and results of operations for the three and
nine months ended March 31, 2009 have been superseded by the documents
incorporated by reference in this prospectus supplement.
In
addition, to the extent that any document or information incorporated by
reference into this prospectus supplement is included in any report on Form 6-K,
Form 40-F, Form 20-F, Form 10-K, Form 10-Q or Form 8-K (or any respective
successor form) that is filed with or furnished to the SEC after the date of
this prospectus supplement, such document or information shall be deemed to be
incorporated by reference as an exhibit to the registration statement of which
this prospectus supplement forms a part. In addition, we may incorporate by
reference into this prospectus supplement other information from documents that
we file with or furnish to the SEC pursuant to Section 13(a) or 15(d) of the US
Securities Exchange Act of 1934, as amended, if and to the extent expressly
provided therein.
Any
statement contained in this prospectus supplement or in a document incorporated
or deemed to be incorporated by reference in this prospectus supplement shall be
deemed to be modified or superseded for purposes of this prospectus supplement
to the extent that a statement contained herein or in any other subsequently
filed document which also is or is deemed to be incorporated by reference herein
modifies or supersedes such statement. The modifying or superseding statement
need not state that it has modified or superseded a prior statement or include
any other information set forth in the document that it modifies or supersedes.
The making of a modifying or superseding statement shall not be deemed an
admission for any purposes that the modified or superseded statement, when made,
constituted a misrepresentation, an untrue statement of a material fact or an
omission to state a material fact that is required to be stated or that is
necessary to make a statement not misleading in light of the circumstances in
which it was made. Any statement so modified or superseded shall not be deemed,
except as so modified or superseded, to constitute a part of this prospectus
supplement.
DOCUMENTS
FILED AS PART OF THE REGISTRATION STATEMENT
In
addition to the documents specified in this prospectus supplement and in the
accompanying prospectus under “Documents Incorporated by Reference”, the form of
sales agreement described in this prospectus supplement has been or will be
filed with the SEC as part of the registration statement on Form F-10 (File No.
333-161783) of which this prospectus supplement forms a part.
YM
BIOSCIENCES INC.
This
summary does not contain all the information about YM BioSciences Inc. that may
be important to you. You should read the more detailed information and financial
statements and related notes that are incorporated by reference into and are
considered to be a part of this prospectus supplement and accompanying
prospectus.
We are a
biopharmaceutical company engaged in the development of drugs and other products
primarily for the treatment of cancer. We in-license substances designed for use
by cancer patients in anti-cancer therapy in order to advance them along the
regulatory and clinical pathways toward commercial approval. We have
three material subsidiaries: (i) YM BioSciences USA Inc., a direct wholly owned
subsidiary incorporated under the laws of Delaware; (ii) CIMYM BioSciences Inc.,
a joint venture subsidiary incorporated under the laws of the Province of
Ontario, 80% of which is owned by us and 20% owned by CIMAB S.A., a Cuban
company responsible for commercializing products developed at Centro de
Inmunología Molecular (Center for Molecular Immunology), Havana, Cuba; and (iii)
YM BioSciences Australia Pty Ltd. (formerly
Cytopia
Limited
)
,
an Australian company we
acquired by merger pursuant to a scheme of arrangement on January 29,
2010.
Our head
office and principal place of business is Suite 400, Building 11, 5045 Orbitor
Drive, Mississauga, Ontario, Canada, L4W 4Y4. Our registered office is 1959
Upper Water Street, Suite 800, Halifax, Nova Scotia, Canada, B3J
2X2.
Our
Products
Our
current portfolio of clinical products includes an anti-cancer agent (a novel
monoclonal antibody, nimotuzumab) in a number of trials currently targeting more
than 10 different tumors and/or stages of cancer as well as a proprietary,
inhalation-delivery approach for fentanyl to treat acute pain including cancer
pain. We recently acquired an oral Janus Kinase (JAK) 1/2 inhibitor as well as a
vascular disrupting agent as part of our acquisition of
YM BioSciences Australia Pty Ltd. (formerly
Cytopia
Limited
)
. See “Recent
Developments”. Three other products, tesmilifene, TGFα vaccine, and
HER-1 vaccine, are not currently expected to advance in clinical development.
The principal targets for the monoclonal antibody are of the most ubiquitous
cancer indications
, including numerous stages of non-small cell lung
cancer, head-and-neck cancer, gastric cancer and glioma (brain cancers), the
latter indication having orphan drug designations in Europe and the US. We
expect, based on clinical trials done to date, to develop our clinical stage
candidates beyond their respective initial indications.
Nimotuzumab
Nimotuzumab
is a humanized monoclonal antibody targeting the epidermal growth factor
receptor (EGFR). The EGFR is present in high concentrations on the surface of
many cancer cells and it is postulated that the binding of ligands to this
receptor is important in the continuing growth of cancer cells. Nimotuzumab
appears to block this binding resulting in the potential for inhibition of cell
growth or, possibly, cell destruction by the immune system. Improved tumor
responses or clinical benefit have been reported when EGFR targeting agents are
combined with other anti-cancer treatments. Our EGFR MAb is being developed to
be administered alone or in combination with other anti-cancer
treatments.
AeroLEF
®
AeroLEF
®
is a proprietary formulation of fentanyl, an opioid analgesic that is
administered by inhalation and permits self-titration by patients. The
development of AeroLEF as a combination of pulmonarily-delivered free and
liposomal dosage form takes advantage of (1) the lung’s large absorptive surface
and thin barrier to absorption to permit rapid transport of the free fentanyl
fraction (loading dose) into the systemic circulation and (2) the capacity of
liposomes to function as reservoirs for the regulated release over time of the
encapsulated fentanyl. AeroLEF’s development is designed to
demonstrate both rapid and extended opioid analgesic levels for patients with
severe and moderate acute pain and, eventually, breakthrough cancer pain.
We continue to prepare
AeroLEF
for further
development internationally. After consulting with regulatory bodies in Europe
and Canada, we are now determining AeroLEF’s optimal clinical path forward and
conducting discussions with potential partners.
CYT387
CYT387 is
an oral JAK1/2 inhibitor, originating from the discovery of JAK1 and JAK2 by Dr.
Andrew Wilks, the founder of Cytopia Limited
(now
YM BioSciences Australia Pty Ltd.)
. A Phase I/II myelofibrosis study
commenced in November 2009 at Mayo Clinic, Rochester, MN, and data on the safety
and tolerability of CYT387 are anticipated in the second half of 2010 for this
debilitating hematological condition
.
CYT997
CYT997, a
vascular disrupting agent (VDA), has dual mechanisms of vascular disruption and
cytotoxicity and has the potential to be broadly active against a range of tumor
types. The drug can be administered both orally and intravenously, which
differentiates it from most other VDAs in development. The agent's oral
bioavailability allows for metronomic administration, which could result in
sustained insult to tumour vasculature, potentially leading to improved
anticancer activity in addition to greater patient convenience over intravenous.
CYT997 is currently in a Phase II single arm study in glioblastoma multiforme, a
deadly form of brain cancer, and preliminary data are expected during
2010.
RECENT
DEVELOPMENTS
On
September 17, 2009, we announced that nimotuzumab had been approved for
marketing in Mexico by CIMAB’s licensee in that country. We also announced that
we had enrolled and treated the first two patients in our multinational
randomized, double-blind trial evaluating nimotuzumab plus whole-brain radiation
therapy (WBRT) against WBRT alone in patients with brain metastases from
non-small cell lung cancer. The trial is designed to enrol approximately 88
patients over 12 months followed by a 12-month follow-up period and will likely
include 12 investigational centers in Canada plus additional centers in other
countries.
On
October 26, 2009, the trading of our common shares on the Alternative Investment
Market of the London Stock Exchange was terminated at our request. Our common
shares had traded on AIM since 2002, but the majority of our shareholder base
and liquidity now result from our Canadian and US listings. Therefore, we
concluded that the additional costs associated with maintaining a listing on AIM
were not justifiable given our North American-focused shareholder
base.
On
December 10, 2009, we announced the first results of a collaborative program
with the National Research Council of Canada’s Biotechnology Research Institute
(NRC-BRI). The program is a multi-target, parallel-discovery research project
funded by us and NRC-BRI to develop our IntelliMab™ technology, a proprietary
platform for generating new therapeutic antibodies that target cell surface
receptors associated with cancer, uniquely optimized to produce efficacy with
reduced toxicities. This collaboration has resulted in a number of antibodies
that bind optimally to HER2/neu-over-expressing breast cancer cells while
minimally binding to HER2 on normal cardiac cells.
On
December 17, 2009, we announced the signing of an agreement with Therapure
Biopharma Inc. pursuant to which Therapure will formulate and fill nimotuzumab
into sterile vials in their aseptic GMP certified and Health Canada licensed
fill suite in Mississauga, Canada. The final product will be utilized by us and
our licensees, Daiichi Sankyo in Japan, Kuhnil in South Korea and Oncoscience AG
in Europe, for all activities, and by Innogene Kalbiotech, our licensee in
Southeast Asia, for global clinical trials. Implementation of the agreement will
occur upon the finalization of an agreed arrangement with the Centre of
Molecular Immunology in Cuba.
On
January 4, 2010, we announced that Rogerio C. Lilenbaum, M.D., M.Sc., Director
of Cancer Research and Director of the Thoracic Oncology Program at the Mt.
Sinai Comprehensive Cancer Center, Miami Beach, Florida, Minesh
Mehta, M.D., a radiation oncologist and professor at the University of Wisconsin
Medical School, and
Roman
Perez-Soler, M.D., Chairman of the Department of Oncology at Montefiore Medical
Center, New York and Director of the Division of Medical Oncology and Professor
of Medicine and Molecular Pharmacology at the Albert Einstein College of
Medicine, together with two additional US oncologists, agreed to constitute a US
consultative committee to us on the ongoing development of nimotuzumab, CYT387
and CYT997.
On
January 11, 2010, we announced the results of a collaboration with researchers
at the University of Toronto for the development of potent antibody-radionuclide
conjugates for use in the treatment of cancer. The approach concluded its first
series of proof-of-principle experiments.
On
January 26, 2010, we announced that the FDA had advised us that we may now enrol
patients at US clinical sites into two on-going randomized, double-blind Phase
II trials of nimotuzumab. This follows the August 10, 2009 grant to our
subsidiary, YM BioSciences USA Inc., of a license by the US Department of
Treasury Office of Foreign Assets Control that lifted the limitation on the
development of nimotuzumab in the US for patients with solid tumor
cancers.
On
January 29, 2010, we completed our acquisition of Cytopia Limited, an Australian
public company based in Melbourne, Australia. The merger was completed pursuant
to a scheme of arrangement under applicable Australian laws. Under the terms of
the merger, we issued 7,276,688 common shares in exchange of all of the issued
and outstanding ordinary shares of Cytopia Limited. See “Prior Sales” In
addition, Mr. Robert G.C. Watson, former Chairman of Cytopia Limited, has been
appointed to our Board of Directors. Mr. Watson has over twenty years experience
as an executive and director of large technology businesses.
On March 9, 2010 Cytopia Limited changed its name to “YM
BioSciences Australia Pty Ltd.”
.
On
February 10, 2010, we announced that we have been granted two additional patents
in the US for AeroLEF, our proprietary, inhaled-delivery composition of free and
liposome-encapsulated fentanyl in development for the treatment of moderate to
severe acute pain. US patent numbers 7,648,981 and 7,648,982 extend the life of
AeroLEF’s patent estate in the US to 2024. We also announced that AeroLEF’s
patent estate has expanded to include other territories with the issuance of
European patent number 1,603,533 and several patent allowances in China, India,
Mexico and other territories.
On March
2, 2010, we made an announcement describing that certain US patents for
nimotuzumab licensed to our majority-owned Canadian subsidiary, CIMYM, have
become subject to a lien in the United States, pursuant to a court order, to a
third party. The lien is a consequence of a dispute unrelated to us, the
licensor, or the patent owner, the Center of Molecular Immunology (CIM). Based
on advice of counsel, we believe that the lien should not affect the exclusive,
royalty-free license for nimotuzumab issued by CIMAB to CIMYM for numerous
territories, including the US. We announced that we do not believe that this
situation will have an impact on our continuing development of nimotuzumab in
the US nor do we expect the development to be material to our
business.
On March
10, 2010, we completed a “registered direct” offering of 14,583,000 million
units at an issue price of $1.20 per unit for gross proceeds of
$17,499,600. Each unit consists of one common share and one-half
common share purchase warrant. Each whole warrant may be exercised to
purchase one common share at US$1.60 from September 10, 2010 until March 10,
2015.
RISK
FACTORS
Investing
in our common shares involves a high degree of risk. You should carefully
consider the risks described below and in the accompanying prospectus before
making an investment decision. You should also refer to the other information in
this prospectus supplement and in the accompanying prospectus, including
information incorporated, or deemed to be incorporated, by reference herein,
including our consolidated financial statements and related notes. The risks and
uncertainties described in this prospectus supplement and the accompanying
prospectus are those that we currently believe may materially affect us.
Additional risks and uncertainties that we are unaware of or that we currently
deem immaterial also may become important factors that affect us. If any of the
following risks actually occurs, our business, financial condition, and results
of operations could be materially adversely affected,
the trading price of our common
shares could decline and you could lose all or part of your investment. Also see
“Risk Factors” beginning on page 7 of the accompanying prospectus.
Risks
Relating To Our Business
The “Risk
Factors” beginning on page
7
of the accompanying prospectus
are incorporated by reference in this prospectus supplement.
The
acquisition of
YM BioSciences Australia Pty Ltd.
(formerly
Cytopia Limited
)
will
result in increased expenditures.
The
acquisition of
YM BioSciences Australia Pty Ltd.
(formerly
Cytopia Limited
)
will
result in an increase of expenditures for the additional staff and resources, as
well as the advancement of the
YM BioSciences
Australia Pty Ltd.
products in clinical development. This will result in
the reduction of our previously anticipated duration of our cash assets. If we
are unsuccessful in our financing efforts, we may have insufficient funds to
complete our clinical development plans as originally anticipated.
We
license products and technologies from Cuba.
The
United States has imposed economic sanctions against Cuba. These sanctions apply
to certain transactions from the United States or activities by a person subject
to US jurisdiction. Among other things, the sanctions prohibit transactions that
involve property in which Cuba or any Cuban national has or has had any interest
whatsoever, direct or indirect.
For
purposes of interpreting the sanctions, ‘‘person subject to US jurisdiction’’
means any US citizen, any US permanent resident alien, any entity organized
under the laws of the United States or any jurisdiction within the United States
(including foreign branches and subsidiaries) or any person in the United
States. We (other than our subsidiary YM USA) are not a person subject to US
jurisdiction for purposes of the sanctions and are not subject to the sanctions
with respect to our activities outside of the United States. However, because
the sanctions prohibit persons subject to US jurisdiction from participating in
financing transactions that would support the Cuban licensed products and
technologies, the proceeds from the sale of our common shares
pursuant to the Sales Agreement
will be used only
to fund drug development activities that do not violate the terms of the Cuba
sanctions.
Nevertheless,
we cannot assure you that OFAC, which administers the US government’s Cuba
sanctions, would agree that the measures we have taken and will take are
sufficient to comply with the sanctions described above.
We are
the exclusive licensee of US, European and other patents related to nimotuzumab
owned by CIMAB, a Cuban company responsible for commercializing products
developed at Cuba’s Centro de Immunologia Molecular, a research institute formed
by the government of Cuba. In connection with a default judgment
obtained from a US federal court in Miami, Florida by an individual claimant
against the Republic of Cuba, the Cuban government and a number of other
parties, including CIMAB, the claimant has recorded a lien against the US
patents that are licensed by us from CIMAB. These are patents US 5,891,996 and
6,506,883, each of which expires in November 2015. The claimant also has
commenced an action to enforce that default judgment. If the claimant
succeeds in its action to enforce the judgment, ownership of the licensed US
patents could be transferred from CIMAB to the claimant or sold to a third
party. Based on the advice of our counsel, we believe that any transfer of the
US patents will be subject to our existing license from CIMAB and that any such
transfer should have no bearing on our rights under the license
agreement. However, there can be no assurance that any subsequent
owner of the US patents will fully cooperate with us in connection with our
efforts to continue the development of nimotuzumab in the United States, will
not attempt to invalidate our license agreement, or will not attempt to take any
other action that could potentially impact our license to the US
patents.
Risks
Relating To This Offering
Our
share price is volatile.
The
market price of our common shares, like that of the securities of many other
biotechnology companies in the development stage, has been, and is likely to
continue to be, highly volatile. This increases the risk of securities
litigation related to such volatility. Factors such as the results of our
preclinical studies and clinical trials, as well as those of our collaborators
or our competitors; other evidence of the safety or effectiveness of our
products or those of our competitors; announcements of technological innovations
or new products by us or our competitors; governmental regulatory actions;
developments with our collaborators; developments (including litigation)
concerning patent or other proprietary rights of our company or our competitors;
concern as to the safety of our products; period-to-period fluctuations in
operating results; changes in estimates of our performance by securities
analysts; market conditions for biotechnology stocks in general; and other
factors not within the control of our company could have a significant adverse
effect on the market price of our common shares.
We
have not paid dividends.
We have
never paid cash dividends on our common shares and do not anticipate paying any
cash dividends in the foreseeable future. We currently intend to
retain our future earnings, if any, to finance further research and the
expansion of our business.
Our
outstanding common shares could be subject to dilution.
The
exercise of stock options and warrants already issued by us and the issuance of
other additional securities in the future, including upon the exercise of the
warrants offered hereby could result in dilution in the value of our common
shares and the voting power represented by the common
shares. Furthermore, to the extent holders of our stock options or
other securities exercise their securities and then sell the common shares they
receive, our share price may decrease due to the additional amount of our common
shares available in the market.
It
may be difficult for non-Canadian investors to obtain and enforce judgments
against us because of our Canadian incorporation and presence.
We are a
corporation existing under the laws of Nova Scotia, Canada. Most of
our directors and officers, and certain of the experts named in the accompanying
prospectus, are residents of Canada or otherwise reside outside the United
States, and all or a substantial portion of their assets, and a substantial
portion of our assets, are located outside the United States. Consequently,
although we have appointed an agent for service of process in the United States,
it may be difficult for holders of these securities who reside in the United
States to effect service within the United States upon those directors and
officers, and the experts who are not residents of the United States. It may
also be difficult for holders of these securities who reside in the United
States to realize in the United States upon judgments of courts of the United
States predicated upon our civil liability and the civil liability of our
directors, officers and experts under the United States federal securities
laws. Investors should not assume that Canadian courts (1) would
enforce judgments of US courts obtained in actions against us or such directors,
officers or experts predicated upon the civil liability provisions of the US
federal securities laws or the securities or “blue sky” laws of any state within
the United States or (2) would enforce, in original actions, liabilities against
us or such directors, officers or experts predicated upon the US federal
securities laws or any such state securities or “blue sky” laws. In addition, we
have been advised by our Canadian counsel that in normal circumstances, only
civil judgments and not other rights arising from United States securities
legislation are enforceable in Canada and that the protections afforded by
Canadian securities laws may not be available to investors in the United
States.
If
there are substantial sales of our common shares, the market price of our common
shares could decline.
Sales of
substantial numbers of our common shares could cause a decline in the market
price of our common shares. Any sales by existing shareholders or holders of
options may have an adverse effect on our ability to raise capital and may
adversely affect the market price of our common shares.
We have broad discretion in
how
we use the net
proceeds of this offering, and we may
not use these proceeds in a manner
desired by our securityholders.
Our
management will have broad discretion with respect to the use of the net
proceeds from this offering and investors will be relying on the judgment of our
management regarding the application of these proceeds. Our management could
spend most of the net proceeds from this offering in ways that our shareholders
may not desire or that do not yield a favourable return. You will not have the
opportunity, as part of your investment in our common shares, to influence the
manner in which the net proceeds of this offering are used. At the date of this
prospectus supplement, we intend to use the net proceeds from this offering to
fund our drug development activities and for general corporate purposes, subject
to the restrictions on our use of the proceeds from the sale of our common
shares to US purchasers. See “Use of Proceeds.” However, our needs may change as
our business and the industry we address evolve. As a result, the proceeds we
receive in this offering may be used in a manner significantly different from
our current expectations.
Because
there is no minimum offering amount required as a condition to closing this
offering, the actual public offering amount and net proceeds to us, if any, from
this offering are not presently determinable and may be substantially less than
the maximum offering amounts set forth above.
We
have adopted a shareholder rights plan which could make it more difficult for a
third party to acquire us, thus potentially depriving our shareholders of a
control premium.
We have
adopted a shareholder rights plan. The provisions of such plan could make it
more difficult for a third party to acquire a majority of our outstanding common
shares, the effect of which may be to deprive our shareholders of a control
premium that might otherwise be realized in connection with an acquisition of
our common shares. See “Description of Share Capital, Common Shares and Related
Information” on page 17 of the accompanying prospectus.
We
expect to be a “passive foreign investment company” for the current taxable
year, which would likely result in materially adverse US federal income tax
consequences for US investors.
We generally
will be designated as a “passive foreign investment company” under the
meaning of Section 1297 of the United States Internal Revenue Code of 1986, as
amended (a "PFIC") if (a) 75% or more of our gross income is “passive income”
(generally, dividends, interest, rents, royalties, and gains from the
disposition of assets producing passive income) in any taxable year, or (b) if
at least 50% or more of the quarterly average value of our assets produce, or
are held for the production of, passive income. US shareholders should be aware
that we believe that we constituted a PFIC during one or more prior taxable
years, and based on current business plans and financial projections, we expect
to be a PFIC for the current taxable year. If we are designated as a PFIC for
any taxable year during which a US person holds our common shares, it would
likely result in materially adverse US federal income tax consequences for such
US person, including, but not limited to, any gain from the sale of our common
shares would be taxed as ordinary income, as opposed to capital gain, and such
gain and certain distributions on our common shares would be subject to an
interest charge, except in certain circumstances. In addition, US persons that
hold common shares should be aware that there can be no assurances that we will
satisfy the record keeping requirements that apply to a PFIC, or that the we
will supply such US shareholders with the information that such US shareholders
require to make certain elections available under the Code that are intended to
mitigate the adverse tax consequences of the PFIC rules with respect to such
common shares, except as otherwise provided in this prospectus supplement. This
paragraph is qualified in its entirety by the discussion below under the heading
“Material United Sates Federal Income Tax Considerations.” The PFIC rules are
extremely complex. A US person holding our common shares is encouraged to
consult a tax adviser regarding the PFIC rules and the US federal income tax
consequences of the acquisition, ownership, and disposition of our common
shares.
EXCHANGE
RATE INFORMATION
In this prospectus supplement, unless
otherwise specified or the context otherwise requires, all dollar amounts are
expressed in US dollars.
The following table sets forth: (i)
the rates of exchange for Canadian dollars, expressed in US dollars, in effect
at the end of the periods indicated; (ii) the average exchange rates in effect
during such periods; (iii) the high rate of exchange in effect during such
periods; and (iv) the low rate of exchange in effect during such periods, such
rates, in each case, based on the noon rates of exchange for conversion of one
Canadian dollar to US dollars as reported by the Bank of
Canada.
|
|
Years
Ended June 30,
|
|
|
Nine
Months Ended
|
|
|
|
2007
|
|
|
2008
|
|
|
2009
|
|
|
March
31, 2010
|
|
Low
|
|
$
|
0.8437
|
|
|
$
|
0.9298
|
|
|
$
|
0.7692
|
|
|
$
|
0.9283
|
|
High
|
|
$
|
0.9452
|
|
|
$
|
1.0905
|
|
|
$
|
0.9984
|
|
|
$
|
0.9938
|
|
Average
|
|
$
|
0.8831
|
|
|
$
|
0.9897
|
|
|
$
|
0.8575
|
|
|
$
|
0.9615
|
|
End
|
|
$
|
0.9404
|
|
|
$
|
0.9817
|
|
|
$
|
0.8602
|
|
|
$
|
0.9844
|
|
On April
23, 2010, the inverse of the noon exchange rate quoted by the Bank of Canada for
Canadian dollars was C$1.00 = US$0.9973.
CONSOLIDATED
CAPITALIZATION
Other
than as described in this prospectus supplement and in the accompanying
prospectus, there have been no material changes in our consolidated
capitalization since December 31, 2009. See “Recent Developments” and
“Prior Sales”.
TRADING
PRICE AND VOLUME
Our
common shares are listed on the TSX under the symbol “YM” and on the NYSE Amex
under the symbol “YMI”. The following table sets forth, for the
periods indicated, the reported high and low prices and the average volume of
trading of our common shares on the TSX and NYSE Amex:
|
|
TSX
(C$)
|
|
|
NYSE
Amex (US$)
|
|
Calendar
period
|
|
High
|
|
|
Low
|
|
|
Daily
Avg.
Volume
|
|
|
High
|
|
|
Low
|
|
|
Daily
Avg.
Volume
|
|
August
2009
|
|
$
|
2.42
|
|
|
$
|
0.63
|
|
|
|
339,875
|
|
|
$
|
2.24
|
|
|
$
|
0.57
|
|
|
|
1,280,856
|
|
September
2009
|
|
$
|
2.14
|
|
|
$
|
1.51
|
|
|
|
139,688
|
|
|
$
|
2.00
|
|
|
$
|
1.40
|
|
|
|
638,972
|
|
October
2009
|
|
$
|
1.65
|
|
|
$
|
1.06
|
|
|
|
61,770
|
|
|
$
|
1.53
|
|
|
$
|
1.03
|
|
|
|
277,620
|
|
November
2009
|
|
$
|
1.76
|
|
|
$
|
1.20
|
|
|
|
90,229
|
|
|
$
|
1.65
|
|
|
$
|
1.12
|
|
|
|
300,907
|
|
December
2009
|
|
$
|
1.46
|
|
|
$
|
1.16
|
|
|
|
25,410
|
|
|
$
|
1.41
|
|
|
$
|
1.11
|
|
|
|
104,067
|
|
January
2010
|
|
$
|
1.99
|
|
|
$
|
1.35
|
|
|
|
108,705
|
|
|
$
|
1.85
|
|
|
$
|
1.27
|
|
|
|
341,618
|
|
February 2010
|
|
$
|
1.85
|
|
|
$
|
1.50
|
|
|
|
29,300
|
|
|
$
|
1.70
|
|
|
$
|
1.42
|
|
|
|
140,775
|
|
March
2010
|
|
$
|
1.53
|
|
|
$
|
1.13
|
|
|
|
149,155
|
|
|
$
|
1.57
|
|
|
$
|
1.10
|
|
|
|
1,009,743
|
|
April
1 to April 23, 2010
|
|
$
|
1.79
|
|
|
$
|
1.17
|
|
|
|
292,083
|
|
|
$
|
1.76
|
|
|
$
|
1.15
|
|
|
|
1,937,289
|
|
PRIOR
SALES
Other
than as set forth below, no common shares or securities exchangeable or
convertible into common shares have been issued during the twelve month period
preceding the date of this prospectus supplement.
On
September 30, 2009, we granted 757,500 options to our employees pursuant to our
stock option plan. Each option is exercisable at a price of $1.58 for a term of
ten years.
On
January 29, 2010, we issued 0.0852 common shares for each common share of
YM BioSciences Australia Pty Ltd. (formerly
Cytopia
Limited
)
held at the record date. This resulted in the
issuance of a total of 7,215,053 common shares. The holders of partly paid
shares of
YM BioSciences Australia Pty Ltd.
(formerly
Cytopia
Limited
)
received 61,635 common shares and 138,442 stock
options as consideration for the exchange of their partly paid shares. In
addition we granted 225,950 stock options to
YM
BioSciences Australia Pty Ltd. (formerly
Cytopia
Limited
)
option holders in consideration for the
cancellation of their
YM BioSciences Australia Pty
Ltd. (formerly
Cytopia
Limited
)
options. The purchase price (value of our
common shares issued plus the fair value of stock options issued in exchange for
the partly paid shares) for
YM BioSciences
Australia Pty Ltd. (formerly
Cytopia
Limited
)
was estimated to be
$12,642,000. The value of the common shares issued was determined using the last
closing price of our common shares on the TSX prior to the acquisition date of
January 29, 2010 of $1.72.
On March
10, 2010, we issued 14,583,000 units, each unit consisting of one common share
and one-half of one common share purchase warrant. Each whole warrant
is exercisable at any time from September 10, 2010 until March 10, 2015 at an
exercise price of $1.60 per share.
On March
18, 2010 and March 22, 2010, we issued 21,100 and 22,000 common shares,
respectively, in connection with the exercise of stock options by certain
employees.
USE
OF PROCEEDS
The net
proceeds from the offering are not determinable in light of the nature of the
distribution. The net proceeds of any given distribution of common
shares through CF&Co in an “at-the-market distribution” will represent the
gross proceeds after deducting the applicable compensation payable to CF&Co
under the sales agreement and expenses of the distribution. We intend
to use any net proceeds from the sale of common shares offered by this
prospectus supplement and the accompanying prospectus to fund our drug
development activities and for general corporate purposes.
The
amounts actually expended for the purposes described above may vary
significantly depending on, among other things, the progress of our research and
development programs, regulatory filings and approvals, technological advances,
activities in anticipation of the commercialization of our products, the terms
of any collaborative or in-licensing arrangements and the status of competitive
products.
Because
the US government has imposed sanctions that prohibit “persons subject to US
jurisdiction” (as that term is explained on page s.9) from participating in
financing transactions that would support our Cuban licensed products and
technologies, we intend to use any net proceeds from the sale of common shares
offered by this prospectus supplement and the accompanying prospectus to fund
our drug development activities not related to Cuba, and to fund general
corporate purposes and overhead save and except for expenses directly related to
nimotuzumab or any other Cuban-related product unless and until specifically
permitted by OFAC. Such proceeds shall be held in segregated accounts to ensure
that they are not used for expenses directly related to nimotuzumab or any other
Cuban-related product.
DETAILS
OF THE OFFERING
Common
Shares
Our
authorized share capital consists of 500,000,000 common shares without nominal
or par value, 500,000,000 Class A non-voting common shares without nominal or
par value, 500,000,000 Class A preferred shares without nominal or par value and
500,000,000 Class B preferred shares, issuable in series, without nominal or par
value. As
of April 23,
2010, there were 77,849,963 common shares, no Class A non-voting common shares
and no Class A or Class B preferred shares outstanding.
All of
the common shares rank equally to voting rights, participation in a distribution
of the assets of our company on a liquidation, dissolution or winding-up of our
company and the entitlement to dividends. The holders of our common shares are
entitled to receive notice of all meetings of shareholders and to attend and
vote the common shares at the meetings. Each common share carries with it the
right to one vote. In the event of the liquidation, dissolution or winding-up of
our company the holders of our common shares will be entitled, subject to the
rights, privileges, restrictions and conditions attaching to any other class of
shares of our company, to receive, on a pro rata basis, share for share, with
the Class A non-voting common shares, all of our remaining property. There are
no pre-emptive or conversion rights and no provisions for redemption,
retraction, purchase for cancellation or surrender or singing or purchase
funds.
PLAN
OF DISTRIBUTION
Sales of
the common shares will be made in transactions that are deemed to be
“at-the-market distributions” as defined in NI 44-102, including sales made
directly on the NYSE Amex or other existing trading markets in the United
States. Subject to the terms and conditions of the sales agreement
and upon instructions from us, CF&Co will solicit offers to purchase our
common shares directly on the NYSE Amex or other existing trading markets in the
United States. We will instruct CF&Co as to the number of common
shares to be sold by them. No common shares will be sold on the TSX
or on other trading markets in Canada as at-the-market
distributions. We or CF&Co may suspend the offering of common
shares upon proper notice and subject to other conditions.
To
compensate CF&Co for their services in acting as agent or as principal in
the sale of common shares, we will pay commission equal to 5.0% of the first
aggregate gross proceeds of US$5 million from sales made pursuant to the sales
agreement. Thereafter we will pay a commission equal to 3.0% of any
subsequent gross proceeds. We estimate that the total expenses that
we will incur for the offering (including fees payable to stock exchanges,
securities regulatory authorities and our counsel and our auditors, but
excluding compensation payable to CF&Co under the terms of the sales
agreement) will be approximately US$175,000.
Settlement
for sales of our common shares will occur on the third business day following
the date on which any sales are made, or on such other date as is industry
practice for regular-way trading, in return for payment of the net proceeds to
us.
In
connection with the sale of the common shares on our behalf, CF&Co will be
deemed to be an “underwriter” within the meaning of the United States Securities
Act of 1933, as amended, and the compensation of CF&Co will be deemed to be
underwriting commissions or discounts. We have agreed to provide
indemnification and contribution to CF&Co against certain civil liabilities,
including liabilities under the United States Securities Act of 1933, as
amended.
The
offering of common shares pursuant to the sales agreement will terminate upon
the earlier of (i) the sale of all common shares subject to the agreement by
CF&Co, and (ii) October 16, 2011. We may also terminate the sales
agreement in our sole discretion at any time by giving 30 days’ notice to
CF&Co. In addition, CF&Co may terminate the sales agreement
under the circumstances specified in the agreement and in its sole discretion at
any time by giving 30 days’ notice to us (except in certain limited
circumstances where a 30 day notice period is not required).
No
underwriter or dealer involved in the offering, no affiliate of such an
underwriter or dealer, and no person or company acting jointly or in concert
with such an underwriter or dealer has over-allotted, or will over-allot, common
shares in connection with the offering or effect any other transaction that are
intended to stabilize or maintain the market price of the common
shares.
The TSX
has conditionally approved the listing of the common shares offered by this
prospectus supplement. Listing is subject to us fulfilling all of the
requirements of the TSX within one business day of the date
hereof. The NYSE Amex has authorized, upon official notice of
issuance, the listing of the common shares offered hereunder.
The
transfer agent for our common shares is Mellon Investor Services LLC in the
United States and CIBC Mellon Trust Company in Canada.
MATERIAL
UNITED STATES FEDERAL INCOME TAX CONSIDERATIONS
The
following is a general summary of the material US federal income tax
consequences applicable to a US Holder (as defined below) arising from and
relating to the acquisition, ownership and disposition of common shares acquired
pursuant to this prospectus supplement.
This
summary is for general information purposes only and does not purport to be a
complete analysis or listing of all potential US federal income tax
considerations that may apply to a US Holder as a result of the acquisition of
common shares pursuant to this prospectus supplement. In addition,
this summary does not take into account the individual facts and circumstances
of any particular US Holder that may affect the US federal income tax
considerations applicable to such US Holder. Accordingly, this
summary is not intended to be, and should not be construed as, legal or US
federal income tax advice with respect to any US Holder. Each US
Holder should consult its own tax adviser regarding the US federal, US state and
local, and foreign tax consequences relating to the acquisition, ownership, and
disposition of common shares.
No ruling
from the US Internal Revenue Service (the “IRS”) or legal opinion has been
requested, or will be obtained, regarding the US. federal income tax
considerations applicable to US Holders as discussed in this
summary. This summary is not binding on the IRS, and the IRS is not
precluded from taking a position that is different from, and contrary to, the
positions taken in this summary. In addition, because the authorities
on which this summary is based are subject to various interpretations, the IRS
and the US courts could disagree with one or more of the positions taken in this
summary.
NOTICE
PURSUANT TO IRS CIRCULAR 230: NOTHING CONTAINED IN THIS SUMMARY CONCERNING ANY
US FEDERAL TAX ISSUE IS INTENDED OR WRITTEN TO BE USED, AND IT CANNOT BE USED,
BY A US HOLDER (AS DEFINED BELOW), FOR THE PURPOSE OF AVOIDING US FEDERAL TAX
PENALTIES UNDER THE CODE (AS DEFINED BELOW). THIS SUMMARY WAS WRITTEN TO SUPPORT
THE PROMOTION OR MARKETING OF THE TRANSACTIONS OR MATTERS ADDRESSED BY THIS
PROSPECTUS SUPPLEMENT. EACH US HOLDER SHOULD SEEK US FEDERAL TAX ADVICE, BASED
ON SUCH US HOLDER’S PARTICULAR CIRCUMSTANCES, FROM AN INDEPENDENT TAX
ADVISOR.
Authorities
This
summary is based on the Internal Revenue Code of 1986, as amended (the “Code”),
Treasury Regulations (whether final, temporary, or proposed), US court
decisions, published IRS rulings, published administrative positions of the IRS,
and the Convention Between Canada and the United States of America with Respect
to Taxes on Income and on Capital, signed September 26, 1980, as amended (the
“Canada-US Tax Convention”), that are applicable and, in each case, as in effect
and available, as of the date of this prospectus supplement. Any of
the authorities on which this summary is based could be changed in a material
and adverse manner at any time, and any such change could be applied on a
retroactive basis and could affect the US federal income tax considerations
described in this summary. This summary does not discuss the
potential effects, whether adverse or beneficial, of any proposed legislation
that, if enacted, could be applied on a retroactive basis.
US
Holders
For
purposes of this summary, a “US Holder” is a beneficial owner of common shares
acquired pursuant to this prospectus supplement that is (a) an individual who is
a citizen or resident of the US for US federal income tax purposes, (b) a
corporation, or other entity classified as a corporation for US federal income
tax purposes, that is created or organized in or under the laws of the US or any
state in the US, including the District of Columbia, (c) an estate if the income
of such estate is subject to US federal income tax regardless of the source of
such income, or (d) a trust if (i) such trust has validly elected to be treated
as a US person for US federal income tax purposes or (ii) a US court is able to
exercise primary supervision over the administration of such trust and one or
more US persons have the authority to control all substantial decisions of such
trust.
Non-US
Holders
For
purposes of this summary, a “Non-US Holder” is a beneficial owner of common
shares that is neither a US Holder nor a partnership. This summary
does not address the US federal income tax considerations applicable to Non-US
Holders relating to the acquisition, ownership, and disposition of common
shares. Accordingly, a Non-US Holder should consult its own tax
adviser regarding the US federal, US state and local, and foreign tax
consequences (including the potential application of and operation of any tax
treaties) relating to the acquisition, ownership, and disposition of common
shares.
US Holders Subject to
Special US Federal Income Tax Rules Not Addressed
This
summary does not address the US federal income tax considerations applicable to
US Holders that are subject to special provisions under the Code, including: (a)
US Holders that are tax-exempt organizations, qualified retirement plans,
individual retirement accounts, or other tax-deferred accounts; (b) US Holders
that are financial institutions, underwriters, insurance companies, real estate
investment trusts, or regulated investment companies or that are broker-dealers,
dealers, or traders in securities or currencies that elect to apply a
mark-to-market accounting method; (c) US Holders that have a “functional
currency” other than the US dollar; (d) US Holders that own common shares as
part of a straddle, hedging transaction, conversion transaction, constructive
sale, or other arrangement involving more than one position; (e) US Holders that
acquired common shares in connection with the exercise of employee stock options
or otherwise as compensation for services; (f) US Holders that hold common
shares other than as a capital asset within the meaning of Section 1221 of the
Code or (g) US Holders that own, directly, indirectly, or by attribution, 10% or
more, by voting power or value, of our outstanding shares. The
summary also does not address the US federal income tax considerations
applicable to US Holders who are (a) US expatriates or former
long-term residents of the US subject to Section 877 of the Code, (b) persons
that have been, are, or will be a resident or deemed to be a resident in Canada
for purposes of the Tax Act; (c) persons that use or hold, will use or hold, or
that are or will be deemed to use or hold, common shares in connection with
carrying on a business in Canada; (d) persons whose common shares constitute
“taxable Canadian property” under the Tax Act; or (e) persons that have a
permanent establishment in Canada for the purposes of the Canada-US Tax
Convention. US Holders and others that are subject to special
provisions under the Code, including US Holders described immediately above,
should consult their own tax advisers.
If an
entity that is classified as partnership (or “pass-through” entity) for US
federal income tax purposes holds common shares, the US federal income tax
consequences applicable to such partnership (or “pass-through” entity) and the
partners of such partnership (or owners of such “pass-through” entity) generally
will depend on the activities of the partnership (or “pass-through” entity) and
the status of such partners (or owners). Partners of entities that
are classified as partnerships (and owners of “pass-through” entities) for US
federal income tax purposes should consult their own tax adviser regarding the
US federal income tax consequences relating to the acquisition, ownership, and
disposition of common shares.
Tax Consequences Other than
US Federal Income Tax Consequences Not Addressed
This
summary does not address the US state and local, US federal estate and gift, US
federal alternative minimum tax, or foreign tax consequences to US Holders
relating to the acquisition, ownership, and disposition of common
shares. Each US Holder should consult its own tax adviser regarding
the US state and local, US federal estate and
gift, US federal alternative
minimum tax and foreign tax consequences relating to the acquisition, ownership,
and disposition of common shares.
Passive Foreign Investment
Company Rules
If we are
considered a “passive foreign investment company” within the meaning of Section
1297 of the Code (a “PFIC”) at any time during a US Holder’s holding period, the
following sections will generally describe the US federal income tax
consequences to US Holders of the acquisition, ownership, and disposition of
common shares.
PFIC
Status
We
generally will be a PFIC under Section 1297 of the Code if, for a tax year, (a)
75% or more of our gross income for such tax year is passive income or (b) 50%
or more of the value of our assets either produce passive income or are held for
the production of passive income, based on the quarterly average of the fair
market value of such assets. “Gross income” generally means all
revenues less the cost of goods sold, and “passive income” includes, for
example, dividends, interest, certain rents and royalties, certain gains from
the sale of stock and securities, and certain gains from commodities
transactions. Active business gains arising from the sale of
commodities generally are excluded from passive income if substantially all of a
foreign corporation’s commodities are (a) stock in trade of such foreign
corporation or other property of a kind which would properly be included in
inventory of such foreign corporation if it is on hand at the close of the
taxable year, or property held by such foreign corporation primarily for sale to
customers in the ordinary course of its trade or business, (b) property used in
the trade or business of such foreign corporation that would be subject to the
allowance for depreciation under Section 167 of the Code, or (c) supplies of a
type regularly used or consumed by such foreign corporation in the ordinary
course of its trade or business.
For
purposes of the PFIC income test and asset test described above, if we own,
directly or indirectly, 25% or more of the total value of the outstanding shares
of another corporation, we will be treated as if it (a) held a proportionate
share of the assets of such other corporation and (b) received directly a
proportionate share of the income of such other corporation. In
addition, for purposes of the PFIC income test and asset test described above,
“passive income” does not include any interest, dividends, rents, or royalties
that are received or accrued by us from a “related person” (as defined in
Section 954(d)(3) of the Code), to the extent such items are properly allocable
to the income of such related person that is not passive income.
Under
certain attribution rules, if we are a PFIC, US Holders will be deemed to own
their proportionate share of any of our subsidiaries which is also a PFIC (a
“Subsidiary PFIC”), and will be subject to US federal income tax on (i) a
distribution on the shares of a Subsidiary PFIC and (ii) a disposition of shares
of a Subsidiary PFIC, both as if the holder directly held the shares of such
Subsidiary PFIC.
We
believe that we constituted a PFIC for one or more prior taxable years, and
based on current business plans and financial projections, we expect that we
will be a PFIC for the current taxable year. The determination of
whether we (or a Subsidiary PFIC) was, or will be, a PFIC for a tax year
depends, in part, on the application of complex US federal income tax rules,
which are subject to differing interpretations. In addition, whether
we (or a Subsidiary PFIC) will be a PFIC for any tax year depends on our assets
and income (and each Subsidiary PFIC) over the course of each such tax year and,
as a result, cannot be predicted with certainty as of the date of this
prospectus supplement. Accordingly, there can be no assurance that
the IRS will not challenge any determination made by us (or a Subsidiary PFIC)
concerning our PFIC status or that we (and each Subsidiary PFIC) were not, or
will not be, a PFIC for any tax year. Each US Holder should consult
its own tax adviser regarding our PFIC status and each Subsidiary
PFIC.
Default PFIC Rules Under
Section 1291 of the Code
If we are
a PFIC, the US federal income tax consequences to a US Holder of the purchase,
ownership, and disposition of common shares will depend on whether such US
Holder is eligible to make and actually makes an
election to treat us (and/or a
Subsidiary PFIC) as a “qualified electing fund” or “QEF” under Section 1295 of
the Code (a “QEF Election”) or has made a mark-to-market election under Section
1296 of the Code (a “Mark-to-Market Election”) with respect to the common
shares. A US Holder that does not make either a QEF Election or a
Mark-to-Market Election will be referred to in this summary as a “Non-Electing
US Holder.”
A
Non-Electing US Holder will be subject to the rules of Section 1291 of the Code
with respect to (a) any gain recognized on the sale or other taxable disposition
of common shares and (b) any excess distribution paid on the common
shares. A distribution generally will be an “excess distribution” to
the extent that such distribution (together with all other distributions
received in the current tax year) exceeds 125% of the average distributions
received during the three preceding tax years (or during a US Holder’s holding
period for the common shares, if shorter).
Under
Section 1291 of the Code, any gain recognized on the sale or other taxable
disposition of common shares of a PFIC (including an indirect disposition of
common shares of a Subsidiary PFIC), and any excess distribution paid on such
common shares (or a distribution by a Subsidiary PFIC to its shareholder that is
deemed to be received by a US Holder) must be rateably allocated to each day of
a Non-Electing US Holder’s holding period for the common shares. The
amount of any such gain or excess distribution allocated to the tax year of
disposition or distribution of the excess distribution and to years before the
entity became a PFIC, if any, would be taxed as ordinary income. The
amounts allocated to any other tax year would be subject to US federal income
tax at the highest tax applicable to ordinary income in each such year, and an
interest charge would be imposed on the tax liability for each such year,
calculated as if such tax liability had been due in each such year. A
Non-Electing US Holder that is not a corporation must treat any such interest
paid as “personal interest,” which is not deductible.
If we are
a PFIC for any tax year during which a Non-Electing US Holder holds common
shares, we will continue to be treated as a PFIC with respect to such
Non-Electing US Holder, regardless of whether our company ceases to be a PFIC in
one or more subsequent years. If we cease to be a PFIC, a
Non-Electing US Holder may terminate this deemed PFIC status with respect to
common shares by electing to recognize gain (which will be taxed under the rules
of Section 1291 of the Code discussed above) as if such common shares were sold
on the last day of the last tax year for which we were a PFIC.
QEF
Election
A US
Holder that makes a QEF Election for the first tax year in which its holding
period of its common shares begins, generally, will not be subject to the rules
of Section 1291 of the Code discussed above with respect to its common
shares. However, a US Holder that makes a QEF Election will be
subject to US federal income tax on such US Holder’s pro rata share of (a) our
net capital gain, which will be taxed as long-term capital gain to such US
Holder, and (b) and our ordinary earnings, which will be taxed as ordinary
income to such US Holder. Generally, “net capital gain” is the excess
of (a) net long-term capital gain over (b) net short-term capital gain, and
“ordinary earnings” are the excess of (a) “earnings and profits” over (b) net
capital gain. A US Holder that makes a QEF Election will be subject
to US federal income tax on such amounts for each tax year in which we are a
PFIC, regardless of whether such amounts are actually distributed to such US
Holder by us. However, for any tax year in which we are a PFIC and
has no net income or gain, US Holders that have made a QEF Election would not
have any income inclusions as a result of the QEF Election. If a US
Holder that made a QEF Election has an income inclusion, such a US Holder may,
subject to certain limitations, elect to defer payment of current US federal
income tax on such amounts, subject to an interest charge. If such US
Holder is not a corporation, any such interest paid will be treated as “personal
interest,” which is not deductible.
A US
Holder that makes a QEF Election generally (a) may receive a tax-free
distribution from us to the extent that such distribution represents our
“earnings and profits” that were previously included in income by the US Holder
because of such QEF Election and (b) will adjust such US Holder’s tax basis in
the common shares to reflect the amount included in income or allowed as a
tax-free distribution because of such QEF Election. In addition, a US
Holder that makes a QEF Election generally will recognize capital gain or loss
on the sale or other taxable disposition of common shares.
The
procedure for making a QEF Election, and the US federal income tax consequences
of making a QEF Election, will depend on whether such QEF Election is
timely. A QEF Election will be treated as “timely” if such QEF
Election is made for the first year in the US Holder’s holding period for the
common shares in which we were a PFIC. A US Holder may make a timely
QEF Election by filing the appropriate QEF Election documents at the time such
US Holder files a US federal income tax return for such year.
A QEF
Election will apply to the tax year for which such QEF Election is made and to
all subsequent tax years, unless such QEF Election is invalidated or terminated
or the IRS consents to revocation of such QEF Election. If a US
Holder makes a QEF Election and, in a subsequent tax year, we cease to be a
PFIC, the QEF Election will remain in effect (although it will not be
applicable) during those tax years in which we are not a
PFIC. Accordingly, if we become a PFIC in another subsequent tax
year, the QEF Election will be effective and the US Holder will be subject to
the QEF rules described above during a subsequent tax year in which we qualify
as a PFIC.
The QEF
Election is made on a shareholder-by-shareholder basis and, once made, can be
revoked only with the consent of the IRS. A US Holder generally makes
a QEF Election by attaching an appropriately completed IRS Form 8621 (Return by
a Shareholder of a Passive Foreign Investment Company or Qualified Electing
Fund), including the information provided in a PFIC annual information
statement, to a timely filed US federal income tax return for the tax year to
which the election relates. Retroactive QEF Elections generally may
be made only by filing a protective statement with such return and if certain
other conditions are met or with the consent of the IRS. In order to
comply with the requirements of a QEF Election, a US Holder must receive certain
information from us.
We will
make available to US Holders, upon their written request, timely and accurate
information as to our company’s status as a PFIC and the status of any
Subsidiary PFIC in which our company owns more than 50% of such Subsidiary
PFIC’s total aggregate voting power, and for each year we are a PFIC, provide to
a US Holder, upon written request, all information and documentation that a US
Holder making a QEF Election with respect to our company and such more than 50%
owned Subsidiary PFIC is required to obtain for US federal income tax
purposes. Because our company may hold 50% or less of the aggregate
voting power of one or more Subsidiary PFICs at any time, US Holders should be
aware that there can be no assurance that our company will satisfy record
keeping requirements that apply to a QEF, or that our company will supply US
Holders with information that such US Holders require to report under the QEF
rules, in the event that our company is a PFIC and a US Holder wishes to make a
QEF Election with respect to any such Subsidiary PFIC. With respect
to Subsidiary PFICs for which our company does not or the US Holders do not
obtain the required information, US Holders will continue to be subject to the
rules discussed above that apply to Non-Electing US Holders with respect to the
taxation of gains and excess distributions. Each US Holder should consult its
own tax advisor regarding the availability of, and procedure for making, a QEF
Election with respect to our company and any Subsidiary PFIC.
Mark-to-Market
Election
A US
Holder may make a Mark-to-Market Election only if the common shares are
marketable stock. The common shares generally will be “marketable
stock” if the common shares are regularly traded on (a) a national securities
exchange that is registered with the SEC, (b) the national market system
established pursuant to section 11A of the Securities and Exchange Act of 1934,
or (c) a foreign securities exchange that is regulated or supervised by a
governmental authority of the country in which the market is located, provided
that (i) such foreign exchange has trading volume, listing, financial
disclosure, and other requirements and the laws of the country in which such
foreign exchange is located, together with the rules of such foreign exchange,
ensure that such requirements are actually enforced and (ii) the rules of such
foreign exchange ensure active trading of listed stocks. If such
stock is traded on such a qualified exchange or other market, such stock
generally will be “regularly traded” for any calendar year during which such
stock is traded, other than in de minimis quantities, on at least 15 days during
each calendar quarter.
A US
Holder that makes a Mark-to-Market Election with respect to its common shares
generally will not be subject to the rules of Section 1291 of the Code discussed
above. However, if a US Holder does not make a Mark-to-Market
Election beginning in the first tax year of such US Holder’s holding period for
the common shares or such
US Holder has not made a timely
QEF Election, the rules of Section 1291 of the Code discussed above will apply
to certain dispositions of, and distributions on, the common shares.
A US
Holder that makes a Mark-to-Market Election will include in ordinary income, for
each tax year in which we are a PFIC, an amount equal to the excess, if any, of
(a) the fair market value of the common shares, as of the close of such tax year
over (b) such US Holder’s tax basis in the common shares. A US Holder
that makes a Mark-to-Market Election will be allowed a deduction in an amount
equal to the excess, if any, of (i) such US Holder’s adjusted tax basis in the
common shares, over (ii) the fair market value of such common shares (but only
to the extent of the net amount of previously included income a result of the
Mark-to-Market Election for prior tax years).
A US
Holder that makes a Mark-to-Market Election generally also will adjust such US
Holder’s tax basis in the common shares to reflect the amount included in gross
income or allowed as a deduction because of such Mark-to-Market
Election. In addition, upon a sale or other taxable disposition of
common shares, a US Holder that makes a Mark-to-Market Election will recognize
ordinary income or loss (not to exceed the excess, if any, of (a) the amount
included in ordinary income because of such Mark-to-Market Election for prior
tax years over (b) the amount allowed as a deduction because of such
Mark-to-Market Election for prior tax years).
A
Mark-to-Market Election applies to the tax year in which such Mark-to-Market
Election is made and to each subsequent tax year, unless the common shares cease
to be “marketable stock” or the IRS consents to revocation of such
election. Each US Holder should consult its own tax adviser regarding
the availability of, and procedure for making, a Mark-to-Market
Election.
Although
a US Holder may be eligible to make a Mark-to-Market Election with respect to
the common shares, no such election may be made with respect to the stock of any
Subsidiary PFIC that a US Holder is treated as owning because such stock is not
marketable. Hence, the Mark-to-Market Election will not be effective
to eliminate the interest charge described above with respect to deemed
dispositions of Subsidiary PFIC stock or distributions from a Subsidiary
PFIC.
Other PFIC
Rules
Under
Section 1291(f) of the Code, the IRS has issued proposed Treasury Regulations
that, subject to certain exceptions, would cause a US Holder that had not made a
timely QEF Election to recognize gain (but not loss) upon certain transfers of
common shares that would otherwise be tax-deferred (e.g., gifts and exchanges
pursuant to corporate reorganizations). However, the specific US
federal income tax consequences to a US Holder may vary based on the manner in
which common shares are transferred.
Certain
additional adverse rules will apply with respect to a US Holder if we are a
PFIC, regardless of whether such US Holder makes a QEF Election. For
example under Section 1298(b)(6) of the Code, a US Holder that uses common
shares as security for a loan will, except as may be provided in Treasury
Regulations, be treated as having made a taxable disposition of such common
shares.
In
addition, a US Holder who acquires common shares from a decedent will not
receive a “step up” in tax basis of such common shares to fair market
value.
Special
rules also apply to the amount of foreign tax credit that a US Holder may claim
on a distribution from a PFIC. Subject to such special rules, foreign taxes paid
with respect to any distribution in respect of stock in a PFIC are generally
eligible for the foreign tax credit. The rules relating to
distributions by a PFIC and their eligibility for the foreign tax credit are
complicated, and a US Holder should consult with their own tax adviser regarding
the availability of the foreign tax credit with respect to distributions by a
PFIC.
The PFIC
rules are complex, and each US Holder should consult its own tax adviser
regarding the PFIC rules and how the PFIC rules may affect the US federal income
tax consequences of the acquisition, ownership, and disposition of common
shares.
US
Federal Income Tax Consequences of the Acquisition, Ownership, and Disposition
of Common Shares
Distributions on Common
Shares
Subject
to the PFIC rules discussed above, a US Holder that receives a distribution,
including a constructive distribution, with respect to a common share will be
required to include the amount of such distribution in gross income as a
dividend (without reduction for any Canadian income tax withheld from such
distribution) to the extent of our current or accumulated “earnings and
profits”, as computed for US federal income tax purposes. To the
extent that a distribution exceeds our current and accumulated “earnings and
profits”, such distribution will be treated first as a tax-free return of
capital to the extent of a US Holder's tax basis in the common shares and
thereafter as gain from the sale or exchange of such common
shares. (See “Sale or Other Taxable Disposition of Common Shares”
below). However, we do not intend to maintain the calculations of
earnings and profits in accordance with US federal income tax principles, and
each US Holder should therefore assume that any distribution by us with respect
to the common share will constitute ordinary dividend income. Dividends received
on common shares generally will not be eligible for the “dividends received
deduction”.
In
addition, dividends received on common shares generally are expected not to be
considered “qualified dividend income”, and thus will not be eligible for the
preferential tax rates applicable to long-term capital gains.
Sale or Other Taxable
Disposition of Common Shares
Subject
to the PFIC rules discussed above, upon the sale or other taxable disposition of
common shares, a US Holder generally will recognize capital gain or loss in an
amount equal to the difference between (i) the amount of cash plus the fair
market value of any property received and (ii) such US Holder’s tax basis in
such common shares sold or otherwise disposed of. While gain or loss recognized
on such sale or other disposition generally would be long-term capital gain or
loss if, at the time of the sale or other disposition, the common shares have
been held for more than one year, the PFIC rules discussed above may render such
gain ordinary income.
Gain or
loss recognized by a US Holder on the sale or other taxable disposition of
common shares generally will be treated as “US source” for purposes of applying
the US foreign tax credit rules unless the gain is subject to tax in Canada and
is resourced as “foreign source” under the Canada-US Tax Convention and such US
Holder elects to treat such gain or loss as “foreign source.” (See
more detailed discussion at “Foreign Tax Credit” below).
Preferential
tax rates apply to long-term capital gain of a US Holder that is an individual,
estate, or trust. There are currently no preferential tax rates for
long-term capital gain of a US Holder that is a
corporation. Deductions for capital losses are subject to significant
limitations under the Code.
Proceeds
paid to a US Holder in foreign currency generally will be taxable as described
below under “Receipt of Foreign Currency”.
Foreign Tax
Credit
A US
Holder who pays (whether directly or through withholding) Canadian income tax
with respect to dividends paid on the common shares generally will be entitled,
at the election of such US Holder, to receive either a deduction or a credit for
such Canadian income tax paid. This election is made on a
year-by-year basis and applies to all foreign taxes paid (whether directly or
through withholding) by a US Holder during a year.
Complex
limitations apply to the foreign tax credit, including the general limitation
that the credit cannot exceed the proportionate share of a US Holder’s US
federal income tax liability that such US Holder’s “foreign source” taxable
income bears to such US Holder’s worldwide taxable income. In
applying this limitation, a US Holder’s various items of income and deduction
must be classified, under complex rules, as either “foreign source” or “US
source.” In addition, this limitation is calculated separately with
respect to specific categories of income. Dividends paid by us
generally will constitute “foreign source” income and generally will be
categorized as “passive category income.”
The foreign tax credit rules are
complex, and each US Holder should consult its own tax adviser regarding the
foreign tax credit rules.
Subject
to certain specific rules, foreign taxes paid with respect to any distribution
in respect of stock in a PFIC are generally eligible for the foreign tax
credit. The rules relating to distributions by a PFIC and their
eligibility for the foreign tax credit are complicated, and a US Holder should
consult with their own tax adviser regarding the availability of the foreign tax
credit with respect to distributions by a PFIC.
Receipt of Foreign
Currency
The
amount of any distribution paid in foreign currency to a US Holder in connection
with the ownership of common shares, or on the sale, exchange or other taxable
disposition of our common shares generally will be equal to the US dollar value
of such foreign currency based on the exchange rate applicable on the date of
actual or constructive receipt (regardless of whether such foreign currency is
converted into US dollars at that time). If the foreign currency
received is not converted into US dollars on the date of receipt, a US Holder
will have a basis in the foreign currency equal to its US dollar value on the
date of receipt. A US Holder that receives foreign currency and
converts such foreign currency into US dollars at a conversion rate other than
the rate in effect on the date of receipt may have a foreign currency exchange
gain or loss, which generally would be treated as US source ordinary income or
loss for foreign tax credit purposes. Each US Holder should consult
its own US tax adviser regarding the US federal income tax consequences of
receiving, owning, and disposing of foreign currency.
Information Reporting;
Backup Withholding Tax
Under US
federal income tax law and Treasury regulations, certain categories of US Holder
must file information returns with respect to their investment in, or
involvement in, a foreign corporation. Penalties for failure to file certain of
these information returns are substantial. US Holders who acquire
common shares through this prospectus supplement and hold common shares should
consult with their own tax advisers regarding the requirements of filing
information returns, and if applicable, any Mark-to-Market Election or QEF
Election.
Payments
made within the US, or by a US payor or US middleman, of dividends on, and
proceeds arising from certain sales or other taxable dispositions of the common
shares may be subject to information reporting and backup withholding tax, at
the rate of 28%, if a US Holder (a) fails to furnish such US Holder’s correct US
social security or other taxpayer identification number (generally on Form W-9),
(b) furnishes an incorrect US taxpayer identification number, (c) is notified by
the IRS that such US Holder has previously failed to properly report items
subject to backup withholding tax, or (d) fails under certain circumstances to
certify, under penalty of perjury, that such US Holder has furnished its correct
US taxpayer identification number and that the IRS has not notified such US
Holder that it is subject to backup withholding tax. However, US
Holders that are corporations generally are excluded from these information
reporting and backup withholding tax rules. Any amounts withheld
under the US backup withholding tax rules will be allowed as a credit against a
US Holder’s US federal income tax liability, if any, or will be refunded, if
such US Holder furnishes required information to the IRS. Each US
Holder should consult its own tax adviser regarding the information reporting
and backup withholding tax rules.
WHERE
YOU CAN FIND MORE INFORMATION
We are a
public company and file annual, quarterly and special reports, proxy statements
and other information with the Canadian securities regulatory authorities and
the SEC. You may read and copy any document we file at the SEC’s public
reference room at 100 F Street, Washington, D.C. 20549. You can request copies
of these documents by writing to the SEC and paying a fee for the copying cost.
Please call the SEC at 1-800-SEC-0330 for more information about the operation
of the public reference room. Our SEC filings are also available to the public
at the SEC’s website at http://www.sec.gov. These documents are also available
through the Internet on the Canadian System for Electronic Document Analysis and
Retrieval (SEDAR) which can be accessed at http://www.sedar.com.
ENFORCEMENT
OF CIVIL LIABILITIES
We are a
corporation existing under the laws of Nova Scotia, Canada. Most of
our directors and officers, and certain of the experts named in this prospectus
supplement and the accompanying prospectus, are residents of Canada or otherwise
reside outside the US, and all or a substantial portion of their assets, and a
substantial portion of our assets, are located outside the US. We have appointed
an agent for service of process in the US, but it may be difficult for holders
of our securities who reside in the US to effect service within the US upon
those directors, officers and experts who are not residents of the US. It may
also be difficult for holders of our securities who reside in the US to realize
in the US upon judgments of courts of the US predicated upon our civil liability
and the civil liability of our directors, officers and experts under the United
States federal securities laws. We have been advised by our Canadian counsel,
Heenan Blaikie LLP, that a judgment of a US court is enforceable in Canada if:
(a) there is a real and substantial connection between the events, persons and
circumstances and the United States judgment such that the US court properly
assumed jurisdiction; (b) the US judgment is final and conclusive; (c) the
defendant was properly served with process from the US court; and (d) the US
substantive or procedural law that led to the judgement is not contrary to
Canadian policy. We are advised that in normal circumstances, only
civil judgments and not other rights arising from US securities legislation are
enforceable in Canada.
We filed
with the SEC, concurrently with our registration statement on Form F-10, an
appointment of agent for service of process on Form F-X. Under the Form F-X, we
appointed DL Services Inc. as our agent.
LEGAL
MATTERS
Certain
legal matters in connection with the common shares offered hereby will be passed
upon for us by Heenan Blaikie LLP, our Canadian counsel, and Dorsey &
Whitney LLP, our US counsel. DLA Piper LLP is US counsel and Blake,
Cassels & Graydon LLP is Canadian counsel for CF&Co in connection with
various matters related to the securities offered hereby. The partners and
associates of Heenan Blaikie LLP as a group, the partners and associates of
Dorsey & Whitney LLP as a group, the partners and associates of DLA Piper
LLP, as a group, and the partners and associates of Blake, Cassels & Graydon
LLP, as a group, each beneficially own, directly or indirectly, less than 1% of
any class of securities issued by us.
No
securities regulatory authority has expressed an opinion about their securities
and it is an offence to claim otherwise.
This short form prospectus
constitutes a public offering of the securities only in those jurisdictions
where they may be lawfully offered for sale and therein only by persons
permitted to sell such securities.
Information has been incorporated by
reference in this short form prospectus from documents filed with the securities
commissions or similar authorities in Canada
. Copies of the documents
incorporated herein by reference may be obtained on request without charge from
the Vice President, Finance and Administration of the issuer at at Suite 400,
Building 11, 5045 Orbitor Drive, Mississauga, Ontario, Canada, L4W 4Y4,
Telephone: (905) 629-9761 and are also available electronically at
www.sedar.com.
SHORT
FORM BASE SHELF PROSPECTUS
New issue
|
September
16, 2009
|
YM
BIOSCIENCES INC.
U.S.$
75,000,000
Common
Shares
Warrants
Units
We may
offer from time to time, during the 25 month period that this short form base
shelf prospectus (including any amendments hereto) (the “prospectus”)
remains effective, up to U.S.$ 75,000,000 in aggregate of common shares (issued
separately or upon exercise of warrants), warrants and units comprising any
combination of the foregoing.
The
specific terms of any securities offered will be described in supplements to
this prospectus. You should read this prospectus and any applicable prospectus
supplement carefully before you invest. This prospectus may not be used to offer
securities unless accompanied by a prospectus supplement.
Our
common shares are listed on the Toronto Stock Exchange (“TSX”) under the symbol
“YM”, on the NYSE Amex under the symbol “YMI” and on the Alternative Investment
Market of the London Stock Exchange (“AIM”) under the symbol
“YMBA”.
Neither
the United States Securities and Exchange Commission (“SEC”) nor any state
securities regulator has approved or disapproved of these securities or
determined if this prospectus is truthful or complete. Any representation to the
contrary is a criminal offence.
We
are permitted, under a multi-jurisdictional disclosure system adopted by the
United States, to prepare this prospectus in accordance with Canadian disclosure
requirements, which are different from those of the United States. We prepare
our financial statements, which are incorporated by reference in this
prospectus, in accordance with Canadian generally accepted accounting
principles, and they are subject to Canadian auditing and auditor independence
standards. Our financial statements may not be comparable to the financial
statements of U.S. companies.
Purchasing
our securities may subject you to tax consequences both in the United States and
Canada. This prospectus or any prospectus supplement may not describe these tax
consequences fully. You should read the tax discussion in any applicable
prospectus supplement fully.
Your
ability to enforce civil liabilities under United States federal securities laws
may be affected adversely because we are incorporated or organized under the
laws of Nova Scotia, Canada, a majority of our directors are not U.S. residents
and a majority of our officers and certain of the experts named in this
prospectus are residents of Canada and a substantial portion of our assets are
located outside the United States.
Our
business and an investment in our securities involve significant risks. See
“Risk Factors”.
No
underwriter has been involved in the preparation of this prospectus or performed
any review of the contents of this prospectus.
This
prospectus contains references to both United States dollars and Canadian
dollars. All dollar amounts referenced, unless otherwise indicated, are
expressed in Canadian dollars. United States dollars are referred to as
“U.S.$”
Our
head office is located at Suite 400, Building 11, 5045 Orbitor Drive,
Mississauga, Ontario, Canada, L4W 4Y4. Our registered office is 1959 Upper Water
Street, Suite 800, Halifax, Nova Scotia, Canada, B3J 2X2.
TABLE
OF CONTENTS
|
Page
|
EXCHANGE
RATES
|
1
|
PRESENTATION
OF FINANCIAL INFORMATION
|
2
|
DOCUMENTS
INCORPORATED BY REFERENCE
|
2
|
ADDITIONAL
INFORMATION
|
3
|
ENFORCEABILITY
OF CIVIL LIABILITIES
|
4
|
SPECIAL
NOTE REGARDING FORWARD-LOOKING STATEMENTS
|
4
|
RISK
FACTORS
|
7
|
PROBABLE
ACQUISITIONS OR OTHER MATERIAL TRANSACTIONS
|
17
|
USE
OF PROCEEDS
|
17
|
DESCRIPTION
OF SHARE CAPITAL, COMMON SHARES AND RELATED
INFORMATION
|
17
|
DESCRIPTION
OF WARRANTS
|
19
|
DESCRIPTION
OF UNITS
|
19
|
PLAN
OF DISTRIBUTION
|
20
|
CERTAIN
INCOME TAX CONSIDERATIONS
|
20
|
AUDITORS
|
20
|
LEGAL
MATTERS
|
20
|
TRANSFER
AGENT AND REGISTRAR
|
21
|
DOCUMENTS
FILED AS PART OF THE REGISTRATION STATEMENT
|
21
|
As used
in this prospectus, the terms “YM”, the “Corporation”, “we”, “our” and “us”
refer to YM BioSciences Inc. and, depending on the context, its consolidated
subsidiaries, and the term “common shares” refers to our common
shares.
EXCHANGE
RATES
The
following table sets out certain exchange rates based upon the noon rate
published by the Bank of Canada. The rates are set out as United States dollars
per CDN$1.00.
|
|
|
|
|
|
|
|
|
|
|
Three Months Ended
|
|
|
|
Years Ended June 30
|
|
|
June 30, 2009
|
|
|
|
2007
|
|
|
2008
|
|
|
2009
|
|
|
|
|
Low
|
|
|
1.058
|
|
|
|
0.917
|
|
|
|
1.002
|
|
|
|
1.083
|
|
High
|
|
|
1.185
|
|
|
|
1.076
|
|
|
|
1.300
|
|
|
|
1.264
|
|
Average
|
|
|
1.132
|
|
|
|
1.010
|
|
|
|
1.166
|
|
|
|
1.167
|
|
On
September 15, 2009, the noon rate quoted by the Bank of Canada was CDN$1.00 =
U.S.$0.9291.
PRESENTATION
OF FINANCIAL INFORMATION
Our
consolidated financial statements have been prepared in accordance with Canadian
generally accepted accounting principles (“Canadian GAAP”). For a description of
the material differences between Canadian GAAP and United States generally
accepted accounting principles (“U.S. GAAP”) as they relate to our financial
statements, see note 17 to our audited consolidated balance sheets as at June
30, 2008 and 2007 and the related consolidated statements of operations and
comprehensive loss and deficit and cash flows for each of the years ended June
30, 2008, 2007 and 2006, incorporated by reference in this
prospectus.
DOCUMENTS
INCORPORATED BY REFERENCE
We are
incorporating by reference in this prospectus certain information contained in
documents filed by us with securities regulatory authorities in Canada. This
means that we are disclosing important information to you by referring you to
those documents. The information incorporated by reference is deemed to be part
of this prospectus, except for any information superseded by information
contained directly in this prospectus or in any other subsequently filed
document which also is or is deemed to be incorporated by reference
herein.
You may
obtain copies of the documents incorporated by reference in this prospectus on
request without charge from our Vice President, Finance and Administration at
Suite 400, Building 11, 5045 Orbitor Drive, Mississauga, Ontario, Canada, L4W
4Y4, Telephone: (905) 629-9761, as well as through the sources described below
under “Additional Information”.
The
following documents are specifically incorporated by reference in this
prospectus:
|
(a)
|
our
annual report filed on the United States Securities and Exchange
Commission (SEC) Form 20-F for the year ended June 30, 2008, dated
September 22, 2008;
|
|
(b)
|
our
audited consolidated balance sheets as at June 30, 2008 and 2007 and the
related consolidated statements of operations and comprehensive loss and
deficit cash flows for each of the years ended June 30, 2008, 2007 and
2006, including the notes thereto and the auditors’ report
thereon;
|
|
(c)
|
management’s
discussion and analysis of our financial condition and results of
operations for the year ended June 30,
2008;
|
|
(d)
|
the
management information circular for the annual and special meeting of
shareholders held on November 20, 2008, as filed on October 30,
2008;
|
|
(e)
|
our
unaudited comparative interim consolidated financial statements as at and
for the three and nine months ended March 31, 2009, including the notes
thereto;
|
|
(f)
|
management’s
discussion and analysis of our financial condition and results of
operations for the three and nine months ended March 31,
2009;
|
All
material change reports (excluding confidential material change reports) and
unaudited interim consolidated financial statements of YM (and management’s
discussion and analysis relating thereto) filed by us with the securities
regulatory authorities in Canada after the date of this prospectus and prior to
the termination of the offering will be deemed to be incorporated by reference
in this prospectus.
When new
documents of the type referred to in the paragraphs above are filed by us with,
and where required accepted, by the securities regulatory authorities in Canada
during the currency of this prospectus, such documents will be deemed to be
incorporated by reference in this prospectus and the previous documents of the
type referred to in the paragraphs above and all material change reports,
unaudited interim consolidated financial statements (and management’s discussion
and analysis relating thereto) and certain prospectus supplements filed by us
with the securities regulatory authorities in Canada before the commencement of
our financial year in which the new documents are filed will no longer be deemed
to be incorporated by reference in this prospectus.
In
addition, to the extent that any document or information incorporated by
reference into this prospectus is included in any report on Form 6-K, Form 40-F,
Form 20-F, Form 10-K, Form 10-Q or Form 8-K (or any respective successor form)
that is filed with or furnished to the SEC after the date of this prospectus,
such document or information shall be deemed to be incorporated by reference as
an exhibit to the registration statement of which this prospectus forms a part.
In addition, we may incorporate by reference into this prospectus, or the
registration statement of which it forms a part, other information from
documents that we file with or furnish to the SEC pursuant to Section 13(a) or
15(d) of the U.S. Securities Exchange Act of 1934, as amended (the “Exchange
Act”), if and to the extent expressly provided therein.
A prospectus supplement containing
the specific terms of any securities offered will be delivered to purchasers of
such securities together with this prospectus and will be deemed to be
incorporated by reference in this prospectus as of the date of the prospectus
supplement solely for the purposes of the offering of securities covered by that
prospectus supplement unless otherwise provided therein
.
Any
statement contained in this prospectus or in a document incorporated or deemed
to be incorporated by reference in this prospectus shall be deemed to be
modified or superseded for purposes of this prospectus to the extent that a
statement contained herein or in any other subsequently filed document which
also is or is deemed to be incorporated by reference herein modifies or
supersedes such statement. The modifying or superseding statement need not state
that it has modified or superseded a prior statement or include any other
information set forth in the document that it modifies or supersedes. The making
of a modifying or superseding statement shall not be deemed an admission for any
purposes that the modified or superseded statement, when made, constituted a
misrepresentation, an untrue statement of a material fact or an omission to
state a material fact that is required to be stated or that is necessary to make
a statement not misleading in light of the circumstances in which it was made.
Any statement so modified or superseded shall not be deemed, except as so
modified or superseded, to constitute a part of this prospectus.
ADDITIONAL
INFORMATION
We have
filed with the SEC a registration statement on Form F-10 of which the prospectus
forms a part. This prospectus does not contain all the information set out in
the registration statement. For further information about us and the securities,
please refer to the registration statement, including the exhibits to the
registration statement.
We are
subject to the information requirements of the Exchange Act and applicable
Canadian securities legislation, and in accordance therewith, we file reports
and other information with the SEC and with the securities regulatory
authorities of certain of the provinces of Canada. Under a multijurisdictional
disclosure system adopted by the United States and Canada, we generally may
prepare these reports and other information in accordance with the disclosure
requirements of Canada. These requirements are different from those of the
United States. As a foreign private issuer, we are exempt from the rules under
the Exchange Act prescribing the furnishing and content of proxy statements, and
our officers, directors and principal shareholders are exempt from the reporting
and shortswing profit recovery provisions contained in Section 16 of the
Exchange Act. In addition, we are not required to publish financial statements
as promptly as United States companies.
The
reports and other information filed by us with the SEC may be read and copied at
the SEC’s public reference room at 100 F Street, N.E., Washington, D.C. 20549.
Copies of the same documents can also be obtained from the public reference room
of the SEC in Washington by paying a fee. Please call the SEC at 1-800-SEC-0330
for further information on the public reference room. The SEC also maintains a
web site (www.sec.gov) that makes available reports and other information that
we file electronically with it, including the registration statement that we
have filed with respect hereto.
Copies of
reports, statements and other information that we file with the Canadian
provincial securities regulatory authorities are electronically available from
the Canadian System for Electronic Document Analysis and Retrieval
(www.sedar.com), which is commonly known by the acronym, “SEDAR”. Reports and
other information about us are also available for inspection at the offices of
the TSX.
ENFORCEABILITY
OF CIVIL LIABILITIES
We are a
corporation existing under the laws of Nova Scotia, Canada. Most of
our directors and officers, and certain of the experts named in this prospectus
are residents of Canada or otherwise reside outside the United States, and all
or a substantial portion of their assets, and a substantial portion of our
assets, are located outside the United States. We have appointed an agent for
service of process in the United States, but it may be difficult for holders of
these securities who reside in the United States to effect service within the
United States upon those directors, officers and experts who are not residents
of the United States. It may also be difficult for holders of these securities
who reside in the United States to realize in the United States upon judgments
of courts of the United States predicated upon our civil liability and the civil
liability of our directors, officers and experts under the United States federal
securities laws.
We have
been advised by our Canadian counsel, Heenan Blaikie LLP, that a judgment of a
United States court may be enforceable in Canada if: (a) there is a real and
substantial connection between the events, persons and circumstances and the
United States proceedings such that the United States court properly assumed
jurisdiction; (b) the United States judgment is final and conclusive; (c) the
defendant was properly served with process from the United States court; and (d)
the United States law that led to the judgment is not contrary to Canadian
public policy, as that term would be applied by a Canadian court. We are advised
that in normal circumstances, only civil judgments and not other rights arising
from United States securities legislation (for example, penal or similar awards
made by a court in a regulatory prosecution or proceeding) are enforceable in
Canada. The enforceability of a United States judgment in Canada will be subject
to the requirements that: (i) an action to enforce the United States judgment
must be commenced in the Ontario Court within any applicable limitation period;
(ii) the Ontario Court has discretion to stay or decline to hear an action on
the United States judgment if the United States judgment is under appeal or
there is another subsisting judgment in any jurisdiction relating to the same
cause of action; (iii) the Ontario Court will render judgment only in Canadian
dollars; and (iv) an action in the Ontario Court on the United States judgment
may be affected by bankruptcy, insolvency or other similar laws affecting the
enforcement of creditors’ rights generally. The enforceability of a United
States judgment in Canada will be subject to the following defences: (i) the
United States judgment was obtained by fraud or in a manner contrary to the
principles of natural justice; (ii) the United States judgment is for a claim
which under Ontario law would be characterized as based on a foreign revenue,
expropriatory, penal or other public law; (iii) the United States judgment is
contrary to Ontario public policy or to an order made by the Attorney General of
Canada under the
Foreign
Extraterritorial Measures Act
(Canada) or by the Competition Tribunal
under the
Competition
Act
(Canada) in respect of certain judgments referred to in these
statutes; and (iv) the United States judgment has been satisfied or is void or
voidable under United States law.
We filed
with the SEC, concurrently with our registration statement on Form F-10, an
appointment of agent for service of process on Form F-X. Under the Form F-X, we
appointed DL Services Inc. as our agent.
SPECIAL
NOTE REGARDING FORWARD-LOOKING STATEMENTS
Statements
contained in this prospectus (including documents incorporated by reference
herein) that are not based on historical fact, including without limitation
statements containing the words "believes," "may," “likely,” "plans," "will,"
"estimate," "continue," "anticipates," "intends," "expects" and similar
expressions, constitute "forward-looking statements" within the meaning of the
United States
Private
Securities Litigation Reform Act of 1995
. Such forward-looking statements
involve known and unknown risks, uncertainties and other factors that may cause
the actual results, events or developments to be materially different from any
future results, events or developments expressed or implied by such
forward-looking statements. Such factors include, without limitation, changing
market conditions, our ability to obtain patent protection and protect our
intellectual property rights, commercialization limitations imposed by
intellectual property rights owned or controlled by third parties, intellectual
property liability rights and liability claims asserted against us, the
successful and timely completion of clinical studies, the impact of competitive
products and pricing, new product development, uncertainties related to the
regulatory approval process, product development delays, our ability to attract
and retain business partners and key personnel, future levels of government
funding, our ability to obtain the capital required for research, operations and
marketing and other risks detailed elsewhere in this prospectus and in the
documents incorporated by reference herein. These forward-looking
statements are based on our beliefs and expectations on the date the statements
are made, and subject to the requirements of applicable securities laws, we
undertake no obligation to publicly update or revise any forward-looking
statements, whether as a result of new information, future events or otherwise.
In light of these risks, uncertainties and assumptions, the forward-looking
events discussed in this prospectus might not occur and you should not place
undue reliance on forward-looking statements. Forward-looking
statements are subject to known and unknown risks, uncertainties and other
factors that may cause our actual results, level of activity, performance or
achievements to be materially different from those expressed or implied by such
forward-looking statements, including:
|
·
|
our
ability to obtain, on satisfactory terms or at all, the capital required
for research, operations and
marketing;
|
|
·
|
general
economic, business and market
conditions;
|
|
·
|
our
ability to successfully and timely complete clinical
studies;
|
|
·
|
product
development delays and other uncertainties related to new product
development;
|
|
·
|
our
ability to attract and retain business partners and key
personnel;
|
|
·
|
the
risk of our inability to profitably commercialize our
products;
|
|
·
|
the
extent of any future losses;
|
|
·
|
the
risk of our inability to establish or manage manufacturing, development or
marketing collaborations;
|
|
·
|
the
risk of delay of, or failure to obtain, necessary regulatory approvals
and, ultimately, product launches;
|
|
·
|
dependence
on third parties for successful commercialization of our
products;
|
|
·
|
inability
to obtain quantities of development product in sufficient quantity or at
standards acceptable to health regulatory authorities to complete clinical
trials or to meet commercial
demand;
|
|
·
|
the
risk of the termination or conversion to non-exclusive licenses or our
inability to enforce our rights under our
licenses;
|
|
·
|
our
ability to obtain patent protection and protect our intellectual property
rights;
|
|
·
|
commercialization
limitations imposed by intellectual property rights owned or controlled by
third parties
|
|
·
|
uncertainty
related to intellectual property liability rights and liability claims
asserted against us;
|
|
·
|
the
uncertainty of recovery of advances to
subsidiaries;
|
|
·
|
the
impact of competitive products and
pricing;
|
|
·
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future
levels of government funding; and
|
|
·
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other
factors discussed under “Risk
Factors”.
|
YM BIOSCIENCES
INC
.
OUR
BUSINESS
We are a
biopharmaceutical company engaged in the development of drugs and other products
primarily for the treatment of patients with cancer. We own or in-license
substances or products in order to advance them along the regulatory and
clinical pathways toward commercial approval.
Our
rights generally cover the major market countries of the developed world
(including Canada, the US, Japan and Europe) or are world-wide. We use our
expertise to manage and perform, within our means, what we believe are the most
critical aspects of the drug development process which include the design and
conduct of clinical trials, the development and execution of strategies for the
protection and maintenance of intellectual property rights and the interaction
with drug regulatory authorities internationally. We concentrate on drug
development and do not engage in drug discovery, avoiding the earlier risk and
investment of time and capital that is generally required before a compound is
identified as appropriate for clinical trials. We both conduct and out-source
clinical trials, and we out-source the manufacture of clinical materials to
third parties.
Our
current portfolio of products in active clinical development includes
nimotuzumab, an anti-cancer agent (monoclonal antibody) which is in a number of
clinical trials currently targeting more than 10 different tumors and/or stages
of cancer, and AeroLEF
®
,
a proprietary, inhalation-delivery approach for fentanyl to treat acute pain
including cancer pain.
We
principally intend to license the rights to manufacture and/or market our
products in development to other pharmaceutical companies in exchange for
license fees and royalty payments and to continue to seek other in-licensing
opportunities in pursuing our business strategy.
OUR
PRODUCTS
We have
two product candidates currently in the clinical stage of
development:
o Nimotuzumab
(previously
known as TheraCIM hR3), a humanized monoclonal antibody, targeting the protein
known as Epidermal Growth Factor Receptor ("EGFr"), is designed to treat
epithelial cancers and to be administered as monotherapy or prior to,
simultaneously with, or subsequent to, chemotherapy and radiotherapy. In various
Phase II trials, the drug has,
inter alia
, improved the
reported response rate to radiation in head-and-neck tumors and demonstrated
clinical benefit in adult and pediatric glioma. The drug has been
approved for sale in India for advanced head and neck cancer, the People’s
Republic of China for nasopharangeal cancer, in the Philippines and Indonesia
for pediatric and adult recurrent glioma, and for head and neck cancer in
Argentina and Columbia, and a number of other countries. Our rights to
nimotuzumab have been sub-licensed to Daiichi-Sankyo Co. Ltd., in Japan,
Oncoscience AG in Germany (“Oncoscience”) for our European territory, to Kuhnil
Pharmaceutical Company for our Korean territory and to Innogene Kalbiotech Ltd.
of Singapore for certain Pacific-rim countries (excluding the People’s Republic
of China) and certain African countries in exchange for license fees and
royalties on commercial sales, if any. Nimotuzumab has been cleared
for use in numerous clinical trials by various regulatory agencies including the
EMEA, Health Canada and the FDA. In August 2009, we received an expected but
important clearance from the US Treasury department to extend our US clinical
program for nimotuzumab, permitting us to conduct trials in any solid tumour
indication.
o AeroLEF
®
,
a proprietary formulation of both free and liposome-encapsulated fentanyl
administered by pulmonary inhalation, is being developed for the treatment of
severe and moderate acute pain and cancer pain. AeroLEF
®
has been developed to provide both rapid onset and extended relief while
recognizing the need for interpersonal variability as well as inter-episode
variability in the amount of drug needed. A randomized, 120-patient
Phase II trial was completed in 2007, a further Phase II was cleared for
initiation by the FDA in 2008, and plans for a Phase III trial have been
discussed with health regulatory agencies in Canada and Europe.
Three
other products, tesmilifene, TGFα vaccine, and HER-1 vaccine are not currently
expected to advance in clinical development.
RISK
FACTORS
An
investment in our securities is speculative and involves a high degree of risk.
Prospective investors should carefully consider, together with other matters
referred to in this prospectus, the following risk factors. If any event arising
from these risks occurs, our business, prospects, financial condition, results
of operations and cash flows could be materially adversely
affected.
Risks Related To Our
Business
We
deal with products that are in the early stages of development and, as a result,
are unable to predict whether we will be able to profitably commercialize our
products.
Since our
incorporation in 1994, none of our products, licensed or owned, has received
regulatory approval for sale in any major market country in which we have an
economic interest in a product. Accordingly, we have not generated any
significant revenues from the product sales. A substantial commitment of
resources to conduct clinical trials and for additional product development will
be required to commercialize most of the products. There can be no assurance
that our remaining products will meet applicable regulatory standards, be
capable of being produced in commercial quantities at reasonable cost or be
successfully marketed, or that the investment made by us in the
commercialization of the products will be recovered through sales, license fees
or related royalties.
We
have few revenues and a history of losses and, therefore, are unable to predict
the extent of any future losses or when or if we will become
profitable.
As at
March 31, 2009, we had an accumulated deficit of $142,987,921 million. We expect
expenditures and the accumulated deficit to increase as we proceed with our
commercialization programs until such time as sales, license fees and royalty
payments, if any, may generate sufficient revenues to fund our continuing
operations. There can be no assurance that the revenues from the
commercialization of our products will be sufficient to support required
expenditures and therefore there can be no assurance of when or if we will
become profitable.
We
depend upon being able to identify promising molecules for licensing or
acquisition and successfully completing the acquisitions or licensing on
economic terms. There is no assurance that we can continue to identify and
license molecules for development.
We do not
conduct basic research of our own. Basic research on a particular
drug product is conducted by other biopharmaceutical companies, scientific and
academic institutions and hospitals, or scientists affiliated with those
institutions. Generally, once the basic research is complete, we enter into
agreements to in-license the right to develop and market the products or acquire
them. We have negotiated certain in-licensing agreements with the University of
Manitoba, CancerCare Manitoba, Vincent Research and Consulting, and CIMAB, S.A.,
a Cuban company responsible for commercializing products developed at the Centro
de Inmunología Molecular (Center for Molecular Immunology) in Havana, Cuba
(“CIMAB”). In addition, AeroLEF
®
technology was developed at Dalhousie University in Halifax, Nova
Scotia.
We
depend upon others for the manufacture, development and sale of our products. If
we are unable to establish or manage collaborations in the future, there could
be a delay in the manufacture, development and sale of our
products.
We enter
into arrangements, with and are dependent on others with respect to, the
manufacture, development and sale of our in-licensed products. Product
development includes, but is not limited to, pre-clinical testing, regulatory
approval processes, clinical testing, and the development of additional
regulatory and marketing information. Our ability to successfully develop and
commercialize our in-licensed products is dependent on our ability to make
arrangements with others on commercially acceptable terms and subject to our
depending upon them to meet regulatory quality standards. The product
development process may be delayed or terminated if we cannot secure or maintain
such arrangements on terms acceptable to us or at all. We do not have long-term,
material, third party manufacturing, formulation or supply agreements, except
with respect to one of our licensed products, nimotuzumab, which is manufactured
in quantities sufficient for clinical testing by CIMAB or a related party,
subject to certain terms and conditions of the licensing agreements between us
and CIMAB and CIMAB has contracted to supply commercial quantities or will
source such supply if, as and when approval for sale has been granted. The
formulation of AeroLEF is manufactured for us by Dalton Pharma Services in
Toronto, Canada in quantities sufficient for clinical trials. YM has
not yet identified an importer in the European Union to test, certify or release
either clinical or commercial supplies.
We
expect to enter into out-licensing agreements with others with respect to the
manufacturing and marketing of our drug products. We may retain co-development
and marketing rights if management determines it appropriate to do
so.
There can
be no assurance that we will be successful in maintaining our relationships with
research institutions or others or in negotiating additional in-licensing or
out-licensing agreements on terms acceptable to us or at all, or that any such
arrangements will be successful. In addition, there can be no assurance that
other parties will not enter into arrangements with such entities for the
development or commercialization of similar products or that the parties with
whom we have made such arrangements will not pursue alternative technologies or
develop products on their own or in collaboration with others, including our
competitors. If we do not establish sufficient in-licensing and out-licensing
arrangements, we may encounter delays in product introductions or may find that
the development, manufacture or sale of our licensed products could be
materially adversely affected.
We
have no experience in commercial manufacturing of our products and may encounter
problems or delays in making arrangements for products to be commercially
manufactured, which could result in delayed development, regulatory approval and
marketing.
We have
not commercially launched any of our licensed or owned products and have no
commercial manufacturing experience with respect to our products. To be
successful, the products must be manufactured in commercial quantities in
compliance with regulatory requirements and at acceptable costs over which we
have no control. We do not have, and do not intend to acquire, facilities for
the production of our products although we may invest in the ownership of
production facilities, or parts of the production process, if appropriate
opportunities are available.
Nimotuzumab
is required to be manufactured in quantities sufficient for clinical testing by
CIMAB or a related party, subject to certain terms and conditions of the
licensing agreements between us and CIMAB. Currently these expectations are
being met. There can be no assurance, however, that such entities will be able
to develop adequate manufacturing capabilities for sufficient commercial scale
quantities in a commercially reasonable manner. In addition, there
are risks that we cannot control regarding the CIMAB manufacturing plant,
including amongst others, events such as weather, fire and other natural
disasters. AeroLEF (which is owned by us)
is a combination of free
and liposome-encapsulated fentanyl. The drug product is manufactured, finished,
and vials are filled, in quantities sufficient for clinical testing. AeroLEF is
currently delivered through a patient-activated nebulizer known as
AeroEclipse
®
and the
devices are purchased by us to be used in clinical trials. The manufacturing
processes for both AeroLEF
drug
product and the AeroEclipse
®
device
are such that we expect that commercial quantities of both can be
manufactured. If the current AeroLEF
supplier
cannot manufacture commercial quantities or we otherwise experience a problem
with the current supplier, it will be necessary for us to obtain AeroLEF
from
a second supplier. The manufacture of AeroLEF
has
been successfully transferred to a second manufacturing source in the US which
may provide clinical material as well as future commercial supply. We
do not have supply agreements with the third-party suppliers of AeroLEF, but
suppliers have produced quantities for us to specification on purchase order. We
expect that we could find new suppliers for AeroLEF, if necessary. There can be
no assurance, however, that we will be able to reach satisfactory arrangements
with our current suppliers or, if necessary, new suppliers or that such
arrangements for either AeroLEF
or
an alternative nebulizing device will be successful. The Corporation has not
clinically tested any nebulizers appropriate for the out-patient market and it
is not known whether any of the products in this category currently available
could be purchased at an economic price or whether the combination of
AeroLEF
in a
portable electronic nebulizer would be safe or effective. All manufacturing
facilities must comply with applicable regulations in their jurisdiction or
where products are to be sold. In addition, production of the licensed and owned
products may require raw materials for which the sources and amount of supply
are limited. An inability to obtain adequate supplies of such raw materials
could significantly delay the development, regulatory approval and marketing of
our licensed and owned products.
We
are dependent on devices from third parties in order to successfully
commercialize AeroLEF.
Third-party
devices will be an important element for successful commercialization of AeroLEF
in both the inpatient and outpatient settings.
We have
selected the AeroEclipse
®
inhalation device for our Phase II clinical studies for the inpatient
indications for AeroLEF and anticipate using the AeroEclipse for further
clinical studies for the inpatient market opportunity. Material changes to the
AeroEclipse device by the manufacturer or a decision to switch to an alternative
inhalation device would likely delay the initiation of later stage clinical
trials. Switching after the initiation of Phase III studies, however, would
require additional clinical trials and could delay the commercialization of
AeroLEF. Currently, YM purchases the AeroEclipse devices and it does not have a
defined supply agreement.
While
inpatient use of AeroLEF, in the hospital or hospice setting, is accomplished
with existing equipment such as the AeroEclipse, outpatient use will require a
portable nebulization device. Several devices currently exist and are otherwise
approved for use with certain respiratory agents (bronchodilators, antibiotics,
steroids). We have established criteria to evaluate and identify the
best devices for use with AeroLEF. Although we would prefer to access these
devices on an arms-length basis from the manufacturer, we will explore the
benefits of a strategic partnership that could provide for custom adaptations to
optimize product delivery, lower prices or other benefits.
The
Drug Enforcement Administration limits the availability of the active
ingredients in certain of our current drug candidates and, as a result, our
quota may not be sufficient to complete clinical trials, or to meet commercial
demand or may result in clinical delays.
The DEA
and similar opioid-regulating agencies of other countries regulate chemical
compounds defined as Schedule I, II, III, IV and V substances, with Schedule I
substances considered to present the highest risk of substance abuse and
Schedule V substances the lowest risk. Certain active ingredients in AeroLEF,
such as fentanyl, are listed by the DEA as Schedule II under the
Controlled Substances Act of
1970
. Consequently, their manufacture, research, shipment, storage, sale
and use are subject to a high degree of oversight and regulation. For example,
all Schedule II drug prescriptions must be signed by a physician, physically
presented to a pharmacist and may not be refilled without a new prescription.
Further, the amount of Schedule II substances we can obtain for clinical trials
and commercial distribution is limited by the DEA and our quota may not be
sufficient to complete clinical trials or meet commercial demand. There is a
risk that DEA regulations may interfere with the supply of the drugs used in our
clinical trials, and, in the future, our ability to produce and distribute our
products in the volume needed to meet commercial demand. Manufacturers for this
product are limited because only those holding a DEA license to manufacture
Schedule II compounds may be considered.
We
are dependent on licenses from third parties and the maintenance of licenses is
necessary for our success.
We have
obtained our rights to the licensed products under license agreements from
various third party licensors as follows:
|
(a)
|
License
Agreement between CIMAB and us dated May 3, 1995 as amended with respect
to nimotuzumab; and
|
|
(b)
|
TGFα
vaccine and HER-1 vaccine dated January 24, 2001;
and
|
|
(c)
|
License
Agreement between the Corporation, the University of Manitoba and The
Manitoba Cancer Treatment and Research Foundation, carrying on its
undertaking as CancerCare Manitoba, dated November 2, 2000 with respect to
tesmilifene.
|
As we own
AeroLEF, there are no license terms.
We depend
upon the license rights to the licensed products for commercialization of the
licensed products. While we believe we are in compliance with our obligations
under the licenses, certain licenses may be terminated or converted to
non-exclusive licenses by the licensors if there is a breach of the terms of the
licenses. There can be no assurance that the licenses are enforceable or will
not be terminated or converted. The termination or conversion of the licenses or
our inability to enforce our rights under the licenses would have a material
adverse effect on our business as we would not have the rights to the products
that we are developing. To the extent that management considers a particular
license to be material to our undertaking, we have entered into a signed license
agreement for that license. Terms of certain remaining licenses are to be
determined at a later date. The in-license agreements to which we are currently
a party require us to maintain and defend the patent rights that we in-license
against third parties.
Although
our current licenses are governed by the laws of Ontario, the enforcement of
certain of them may necessitate pursuing legal proceedings and obtaining orders
in other jurisdictions, including the US and the Republic of Cuba. There can be
no assurance that a court judgment or order obtained in one jurisdiction will be
enforceable in another. In international venture undertakings it is standard
practice to attorn to a neutral jurisdiction to seek remedy for unresolved
commercial disputes. These arrangements are usually negotiated as part of the
original business agreement. In the case of the license agreements with us, the
parties have agreed that the law governing the agreements is Ontario law and the
parties will attorn to the courts of Ontario or the Federal court of Canada to
resolve any dispute regarding the agreements.
One of
our products in clinical development is licensed from Cuba. The commercial and
legal environment in Cuba is in a formative stage and may be subject to
political risk. It is possible that we may not be able to enforce our legal
rights in Cuba or against Cuban entities to the same extent that we would be
able to do in a country with a more established commercial and legal system.
Termination of our license arrangements or difficulties in enforcement of such
arrangements could have a material adverse effect on our ability to continue
development of our licensed products from that country.
We have a
number of license agreements with CIMAB. CIMAB is a corporation owned by an
institution of the Government of Cuba that purportedly operates at arms-length
from the state bureaucracy with regard to its business, scientific and
administrative decision-making. CIMAB is reportedly akin to a “crown
corporation” in Canada. CIMAB’s management is purportedly both autonomous and
responsible for the success of its business decisions. Despite the fact that
CIMAB’s management is purportedly both autonomous and responsible for business
decisions and that the license agreements with us declare Ontario law as the
governing law, because of the fact that CIMAB is ultimately a state-owned entity
we will not necessarily be able to enforce compliance by CIMAB with any judgment
if CIMAB or the Government of Cuba refuses to comply.
Although
all of the funds advanced to our joint venture subsidiaries have been expensed,
we are only entitled to recover those expenditures when the joint venture’s net
income exceeds the amount of cumulative advances.
YM and
CIMAB entered into a funding agreement with CIMYM (now CIMYM BioSciences Inc.)
in November 1995 (the “Funding Agreement”) in connection with the 1995 CIMYM
license with respect to nimotuzumab. The Funding Agreement provides that we will
arrange for the appropriate studies and clinical trials for the licensed
products held by CIMYM BioSciences Inc. and will fund the cost of such studies
and trials provided that doing so would not be commercially or scientifically
unreasonable. Accordingly, we make the final determination as to whether or not
a clinical trial expense is justified with respect to any given
product.
We are
entitled to reimbursement of all advances made by us pursuant to the Funding
Agreement, from the results of the successful development of the licensed
products and generation of income. CIMYM BioSciences repays such advances
out of a portion of its revenues in priority to eventual revenue or
profit sharing arrangements under the 1995 CIMYM License.
As at
March 31, 2009, we had advanced $46,051,082 to CIMYM BioSciences. Since we have
expensed the total amount no further accounting for those advances would affect
our balance sheet or income statement and any reimbursement of such advances
would be considered to be income by us.
We
are reliant on licensors and others for research on new products.
We do not
conduct our own basic research with respect to the identification of new
products. Instead, we review and analyze research and development work conducted
by others as a primary source for new products. While we expect that we will be
able to continue to identify licensable products or research suitable for
licensing and commercialization by us, there can be no assurance that useful
products will be available to us on commercially acceptable
terms.
We
conduct our development internationally and are subject to laws and regulations
of several countries which may affect our ability to access regulatory agencies
and may affect the enforceability and value of our licenses.
Clinical
trials on our development products have been conducted by us and our
sub-licensees in more than 20 countries including Canada, across the United
Kingdom, the European Union, Japan, Germany, India, Indonesia, Korea, Russia and
the US and we intend to, and may, conduct future clinical trials in these and
other jurisdictions. There can be no assurance that any sovereign government,
including Canada’s, will not establish laws or regulations that will be
deleterious to our interests. There is no assurance that we, as a Canadian
corporation, will continue to have access to the regulatory agencies in any
jurisdiction where we might want to conduct clinical trials or obtain final
regulatory approval, and there can be no assurance that we will be able to
enforce our licenses in foreign jurisdictions. Governments have, from time to
time, established foreign exchange controls which could have a material adverse
effect on our business and financial condition, since such controls may limit
our ability to flow funds into a particular country to meet our obligations
under in-licensing agreements, and to flow funds which we may be entitled to, in
the form of royalty and milestone payments, under out-licensing agreements out
of a particular country In addition, the value of our licenses will
depend upon the absence of punitive or prohibitive legislation in respect of
biological materials.
We
also conduct our in-licensing internationally and we currently own or license
products and technologies from sources in Canada and Cuba. We have previously
licensed, and intend to and may license, products from sources in other
jurisdictions.
We have
licensed nimotuzumab from CIMAB, a corporation representing a scientific
institute in Cuba. The US has maintained an embargo against Cuba, administered
by the US Department of Treasury. The laws and regulations establishing the
embargo have been amended from time to time, most recently by the passage of the
Cuban Liberty and Democratic Solidarity Act (the “Helms-Burton Act”). The
embargo applies to almost all transactions involving Cuba or Cuban enterprises,
and it bars from such transactions any US persons unless such persons obtain
specific licenses from the US Department of Treasury authorizing their
participation in the transactions. There is Canadian legislation (the Foreign
Extraterritorial Measures Act) which provides generally that judgments against
Canadian companies under the Helms-Burton Act will not be enforceable in Canada.
The US embargo could have the effect of limiting our access to US capital, US
financing, US customers and US suppliers. In particular, our products licensed
from Cuban sources, noted above, are likely to be prohibited from being licensed
or sold in the US unless the US Department of Treasury issues a license or the
embargo is lifted.
The
Helms-Burton Act authorizes private lawsuits for damages against anyone who
“traffics” in property confiscated, without compensation, by the Government of
Cuba from persons who at the time were, or have since become, nationals of the
US. We do not own any real property in Cuba and, to the best of our knowledge,
and based upon the advice of the Cuban government, none of the properties of the
scientific centers of the licensors in which the licensed products were
developed and are or may be manufactured was confiscated by the Government of
Cuba from persons who at the time were, or have since become, nationals of the
US. However, there can be no assurance that this is correct.
Risks Related To Our
Financial Results And Need For Financing
We
expect to be a “passive foreign investment company” for the current taxable
year, which would likely result in materially adverse US federal income tax
consequences for US investors.
We will
be designated as a “passive foreign investment company” under the meaning of
Section 1297 of the United States Internal Revenue Code of 1986, as amended (a
"PFIC") if (a) 75% or more of our gross income is “passive income” (generally,
dividends, interest, rents, royalties, and gains from the disposition of assets
producing passive income) in any taxable year, or (b) if at least 50% of the
average value of our assets produce, or are held for the production of, passive
income. US shareholders should be aware that we believe that we constituted a
PFIC during one or more prior taxable years, and based on current business plans
and financial projections, we expect to be a PFIC for the current taxable year.
If we are designated as a PFIC for any taxable year during which a US
shareholder holds our common shares, it would likely result in materially
adverse US federal income tax consequences for such US shareholder, including,
but not limited to, any gain from the sale of our common shares would be taxed
as ordinary income, as opposed to capital gain, and such gain and certain
distributions on our common shares would be subject to an interest charge,
except in certain circumstances. In addition, US shareholders should be aware
that there can be no assurances that the Corporation will satisfy the record
keeping requirements that apply to a PFIC, or that the Corporation will supply
US shareholders with the information that such US shareholders require to make
certain elections available under the Code that are intended to mitigate the
adverse tax consequences of the PFIC rules. The PFIC rules are extremely
complex. A US shareholder of our common shares is encouraged to consult a tax
advisor regarding the PFIC Rules and the US federal income tax consequences of
the acquisition, ownership, and disposition of our common shares.
We
may not be able to obtain necessary funding from sales, license fees, milestones
or royalties and, as a result, may need to try to obtain capital through the
public market or private financing which may not be available on acceptable
terms, or at all.
We will
require additional funding for the commercialization of our products, licensed
and owned, and if new products are licensed or acquired and put into
development. The amount of additional funding required depends on the status of
each project or new opportunity at any given time. Our business strategy is to
in-license rights to promising products, further develop those products by
progressing the products toward regulatory approval by conducting and managing
clinical trials, and finally, generally, to out-license rights to manufacture
and/or market resulting products to other pharmaceutical firms generally in
exchange for royalties and license fees. Due to the in- and out-licensing
arrangements and our dependence on others for the manufacture, development and
sale of our in-licensed products, we do not have consistent monthly or quarterly
expenditures and cannot determine the amount and timing of required additional
funding with any certainty. As at March 31, 2009 we had cash and short-term
deposits totalling $46.7 million and accounts payables and accrued liabilities
of $1.9 million.
We assess
our additional funding needs on a project-by-project basis from time-to-time. To
the extent that we are unable to fund our expenditures from sales, license fees
and royalties, it will be necessary to reconsider whether to continue existing
projects or enter into new projects, or to access either the public markets or
private financings if conditions permit. In addition, we have no established
bank financing arrangements and there can be no assurance that we will be able
to establish such arrangements on satisfactory terms or at all. Such financing,
if required and completed, may have a dilutive effect on the holders of our
common shares. There is no assurance that such financing will be available if
required or that it will be available on favorable terms.
Our
operating results and stock price may fluctuate significantly.
The
trading price of our common shares, as with many pharmaceutical and
biotechnology companies, has historically been and is likely to remain highly
volatile. The market has from time to time experienced significant
price and volume fluctuations that are unrelated to the operating performance of
particular companies. Factors such as the efficacy and safety of our
products or the products of our competitors, announcements of technological
innovations by us or our competitors, governmental regulations, developments in
our patents or other proprietary rights, our licensors or our competitors,
litigation, fluctuations in our operating results, thin capitalization, market
conditions for biopharmaceutical stocks and general market and economic
conditions could have a significant impact on the future trading price of our
common shares. In addition, the price of our common shares is highly volatile
since it may take years before any of our licensed products will receive final
regulatory approval to be marketed in Canada, the US or other territories, if at
all.
There
is no assurance that an active trading market in our common shares will be
sustained.
Our
common shares are listed for trading on the TSX, NYSE Amex and on the AIM.
However, there can be no assurance that an active trading market in our common
shares on these stock exchanges will be sustained.
We
are susceptible to general economic conditions
The year
2008 was marked by global economic turmoil. Economic conditions worsened over
the course of the year and into 2009. Recent economic projections by various
governmental and other agencies have predicted that negative economic conditions
may extend throughout 2009 and into 2010. General economic conditions may have a
significant impact on YM, including our commercialization opportunities, our
ability to raise financing and our ability to work with others upon whom we rely
for basic research, manufacture, development and sale of our
products.
Risks Related To Our
Industry
If
our clinical testing of drug products do not produce successful results, we will
not be able to commercialize our products.
Each of
our products, licensed or owned, must be subjected to additional clinical
testing in order to demonstrate the safety and efficacy of our products in
humans. Our ability to commercialize our products will depend on the success of
currently ongoing clinical trials and subsequent clinical trials that have not
yet begun.
We are
not able to predict the results of pre-clinical and clinical testing of our drug
products. It is not possible to predict, based on studies or testing in
laboratory conditions or in animals, whether a drug product will prove to be
safe or effective in humans. Further, preclinical data may not be sufficient for
regulators to accept positive clinical data for approval to commercialize a
product. Pre-clinical data must have been conducted to high regulatory standards
and may be found, on review by health regulatory authorities, to be of
insufficient quality to support an application for commercialization of our
products. In addition, success in one stage of testing is not necessarily an
indication that the particular drug product will succeed in later stages of
testing and development. There can be no assurance that the pre-clinical or
clinical testing of our products will yield satisfactory results that will
enable us to progress toward commercialization of such products. Unsatisfactory
results may have a material adverse effect on our business, financial condition
or results of operations as they could result in us having to reduce or abandon
future testing or commercialization of particular drug products.
If
our competitors develop and market products that are more effective than our
existing product candidates or any products that we may develop, or obtain
marketing approval before we do, our products may be rendered obsolete or
uncompetitive.
Technological
competition from pharmaceutical companies, biotechnology companies and
universities is intense and is expected to increase. Many of our competitors and
potential competitors have substantially greater product development
capabilities and financial, scientific, marketing and human resources than we
have. Our future success depends in part on our ability to maintain a
competitive position, including our ability to further progress our products,
licensed or owned, through the necessary pre-clinical and clinical trials
towards regulatory approval for sale and commercialization. Other companies may
succeed in commercializing products earlier than we are able to commercialize
our products or they may succeed in developing products that are more effective
than our products. We consider our main competitors to be: Amgen, AstraZeneca,
BMS, Roche, Eli Lilly, Genentech, Genmab, Merck KGaA and OSI with respect to
nimotuzumab. The main competitors, to our knowledge, for the AeroLEF product are
Cephalon, Endo, Akela, Alexza, Aradigm, Teva, BDSI, Paion and Alza.
Our
success depends in part on developing and maintaining a competitive position in
the development and commercialization of our products, licensed or owned, and
technological capabilities in our areas of expertise. The biotechnology and
pharmaceutical industries are subject to rapid and substantial technological
change. While we will seek to expand our technological capabilities in order to
remain competitive, there can be no assurance that developments by others will
not render our products non-competitive or that we or our licensors will be able
to keep pace with technological developments. Competitors have developed
technologies that could be the basis for competitive products. Some of those
products may have an entirely different approach or means of accomplishing the
desired therapeutic effect than our products and may be more effective or less
costly than our products. In addition, other forms of medical treatment may
offer competition to the products. The success of our competitors and
their products and technologies relative to our technological capabilities and
competitiveness could have a material adverse effect on the future pre-clinical
and clinical trials of our products, including our ability to obtain the
necessary regulatory approvals for the conduct of such trials.
We
are subject to extensive government regulation that increases the cost and
uncertainty associated with gaining final regulatory approval of our product
candidates.
Securing
final regulatory approval for the manufacture and sale of human therapeutic
products in Canada and our other markets, including the US, is a long and costly
process that is controlled by that particular country’s national regulatory
agency. The national regulatory agency in Canada is Health Canada, in Europe it
is the EMEA and in the US it is the FDA. Other national regulatory agencies have
similar regulatory approval processes, but each is different. Approval in
Canada, Europe, or the US does not assure approval by other national regulatory
agencies, although often test results from one country may be used in
applications for regulatory approval in another country.
Prior to
obtaining final regulatory approval to market a drug product, every national
regulatory agency has a variety of statutes and regulations which govern the
principal development activities. These laws require controlled research and
testing of products, government review and approval of a submission containing
pre-clinical and clinical data establishing the safety and efficacy of the
product for each use sought, approval of manufacturing facilities including
adherence to good manufacturing practices during production and storage, and
control of marketing activities, including advertising and
labelling.
None of
our products have been completely developed or tested and, therefore, we are not
yet in a position to seek final regulatory approval to market any of our
products. To date we have obtained various regulatory clearances to develop and
test our products. Nimotuzumab has been cleared for testing in the US, Canada,
Europe, Japan, Korea, and Indonesia/Malaysia/Singapore and has been designated
as an orphan drug for certain indications in Europe and the US. It is in Phase
II and III trials in certain of those territories. Trials of AeroLEF have
concluded a Phase I, IIa and IIb in Canada, a Phase II has been cleared for
initiation in the US and a Phase III is currently being designed.
Nimotuzumab,
which is being developed in Canada, the US, Europe, Japan, Korea, certain
African countries and Southeast Asian countries sub-licensed by YM is also being
separately developed, tested, or marketed in Argentina, Brazil, China, Colombia,
Cuba, India, and Peru, amongst others. The US established an embargo against
Cuba in 1961, reinforced by the Helms-Burton Act in 1996, and Cuba is among
several nations which have been identified by the US Department of State as
being a state sponsoring terrorism. As such the US Government has put in place
certain limitations on conduct of business with Cuba and anti-terrorism
legislation against Cuba. Although, as of the date of this filing such
anti-terrorism controls have not had any adverse effect on our operations,
because of the anti-terrorism controls and the Helms-Burton Act, there is no
assurance that the Corporation will be able to complete clinical testing in the
US or obtain OFAC or final regulatory approval in order to successfully
commercialize our nimotuzumab in the US. We were successful in September 2006 in
our application for a Special License to import nimotuzumab for a clinical trial
in the US and received clearance for this trial from the FDA in certain of these
territories following the fiscal 2007 year end. In August 2009, we received an
expected but important clearance from the US Treasury department to extend our
US clinical program for nimotuzumab, permitting us to conduct trials in any
cancer indication.
There can
be no assurance that the licensed products will be successfully commercialized.
The process of completing clinical testing and obtaining final regulatory
approval to market the licensed products is likely to take a number of years for
most of the licensed products and require the expenditure of substantial
resources. Any failure to obtain, or a delay in obtaining, such approvals could
adversely affect our ability to develop the product and delay commercialization
of the product. Further, there can be no assurance that our licensed products
will prove to be safe and effective in clinical trials under the standards of
the regulations in our territories or receive applicable regulatory approvals
from applicable regulatory bodies.
Changes
in government regulations although beyond our control could have an adverse
effect on our business.
We have,
or have had, licenses with, or clinical trials at, various academic
organizations, hospitals and companies in Canada, Cuba, India, Italy, Japan,
Korea, Germany, the US, the United Kingdom, countries in Southeast Asia, and
other countries and we depend upon the validity of our licenses and access to
the data for the timely completion of clinical research in those jurisdictions.
Any changes in the drug development regulatory environment or shifts in
political attitudes of a government are beyond our control and may adversely
affect our business.
Our
business may also be affected in varying degrees by such factors as government
regulations with respect to intellectual property, regulation or export
controls. Such changes remain beyond our control and the effect of any such
changes cannot be predicted.
These
factors could have a material adverse effect on our ability to further develop
our licensed products.
Risks Related To
Intellectual Property And Litigation
Our
success depends upon our ability to protect our intellectual property and our
proprietary technology.
Our
success will depend, in part, on our ability and our licensors’ ability to
obtain patents, maintain trade secrets protection, and operate without
infringing on the proprietary rights of third parties or having third parties
circumvent our rights. Certain licensors and the institutions that they
represent, and in certain cases, us on behalf of the licensors and the
institutions that they represent, have filed and are actively pursuing certain
applications for Canadian and foreign patents. The patent position of
pharmaceutical and biotechnology firms is uncertain and involves complex legal
and financial questions for which, in some cases, certain important legal
principles remain unresolved. There can be no assurance that the patent
applications made in respect of the owned or licensed products will result in
the issuance of patents, that the term of a patent will be extendable after it
expires in due course, that the licensors or the institutions that they
represent will develop additional proprietary products that are patentable, that
any patent issued to the licensors or us will provide us with any competitive
advantages, that the patents of others will not impede our ability to do
business or that third parties will not be able to circumvent or successfully
challenge the patents obtained in respect of the licensed products. The cost of
obtaining and maintaining patents is high. Furthermore, there can be no
assurance that others will not independently develop similar products which
duplicate any of the licensed products, or, if patents are issued, design around
the patent for the product. There can be no assurance that our processes or
products or those of our licensors do not or will not infringe upon the patents
of third parties, or that the scope of our patents or those of our licensors
will successfully prevent third parties from developing similar and competitive
products.
Much of
our know-how and technology may not be patentable, though they may constitute
trade secrets. There can be no assurance, however, that we will be able to
meaningfully protect our trade secrets. To help protect our intellectual
property rights and proprietary technology we require employees, consultants,
advisors and collaborators to enter into confidentiality agreements. There can
be no assurance that these agreements will provide meaningful protection for our
trade secrets, know-how or other proprietary information in the event of any
unauthorized use or disclosure.
We
maintain patents in connection with nimotuzumab, AeroLEF and tesmilifene. The
following is a description of our key current and pending patents in connection
with these drug products.
Nimotuzumab
CIMYM is
the exclusive licensee for particular territories including the US under a
patent estate that includes composition of matter coverage for nimotuzumab, and
further includes coverage for nimotuzumab-based formulations and end-uses in the
treatment of EGFR-dependent cancers. Patents are granted in the US, Europe,
Japan, and Canada.
CIMYM’s
key US patent, US 5,891,996 expires in November 2015, and term extensions of up
to five years may be available under the Patent Term Restoration Act. The same
term and extension apply also to the key European patent, EP
712863.
There may
also be risks related to nimotuzumab as our license originates from
Cuba. Cuba is a formally socialist country and, under the current
patent law, ownership of the inventions of the Cuban inventors for which patent
applications have been filed rests with the State. The material license
agreement for our Cuban sourced products is a license agreement between us and
CIMAB, dated May 3, 1995, as amended, with respect to nimotuzumab. There is no
guarantee that, with any future changes in the political regime, the Cuban
government would continue to honour such a license agreement.
AeroLEF
®
The
AeroLEF product is described in four patent families. We own key patents,
expiring in 2014, claiming a method of administering systemic analgesia by
inhaling free and liposome-encapsulated opioid analgesic. North American
coverage includes a reissued US patent and a Canadian patent. We also own two US
applications with counterpart PCT applications now filed in all countries of
interest. The term of patents issuing from these applications expires
in 2024. These applications claim the formulation for use in a method
comprised of continuously inhaling the formulation to deposit at least one
rapid-onset opioid and one sustained-effect opioid in the lungs to avoid the
onset of side effects. The patent has been accepted in Europe, and is validated
in all important European countries. Another PCT application, now filed in all
countries of interest and entitled “Stable Compositions”, claims the
manufacturing method and other physical characteristics of the
formulation.
Our
potential involvement in intellectual property litigation could negatively
affect our business.
Our
future success and competitive position depend in part upon our ability to
maintain our intellectual property portfolio. There can be no assurance that any
patents will be issued on any existing or future patent applications. Even if
such patents are issued, there can be no assurance that any patents issued or
licensed to us will not be challenged. Our ability to establish and maintain a
competitive position may be achieved in part by prosecuting claims against
others who we believe are infringing our rights and by defending claims brought
by others who believe that we are infringing their rights. In addition,
enforcement of our patents in foreign jurisdictions will depend on the legal
procedures in those jurisdictions. Even if such claims are found to be invalid,
our involvement in intellectual property litigation could have a material
adverse effect on our ability to out-license any products that are the subject
of such litigation. In addition, our involvement in intellectual property
litigation could result in significant expense, which could materially adversely
affect the use or licensing of related intellectual property and divert the
efforts of our valuable technical and management personnel from their principal
responsibilities, whether or not such litigation is resolved in our
favor.
Product
liability claims are an inherent risk of our business, and if our clinical trial
and product liability insurance prove inadequate, product liability claims may
harm our business.
Human
therapeutic products involve an inherent risk of product liability claims and
associated adverse publicity. We currently maintain clinical trial liability
insurance with an ultimate net loss value of up to $10 million per claim and a
policy aggregate of $10 million (except for AeroLEF which has a limit of $5
million per claim and a policy aggregate of $5 million). We currently have no
other product liability insurance and there can be no assurance that we will be
able to obtain or maintain product liability insurance on acceptable terms or
with adequate coverage against potential liabilities. Such insurance is
expensive, difficult to obtain and may not be available in the future on
acceptable terms, or at all. An inability to obtain sufficient insurance
coverage on reasonable terms or to otherwise protect against potential product
liability claims could have a material adverse effect on our business by
preventing or inhibiting the commercialization of our products, licensed and
owned, if a product is withdrawn or a product liability claim is brought against
us.
Risks Related To Being A
Canadian Entity
We
are governed by the corporate laws in Nova Scotia, Canada which in some cases
have a different effect on shareholders than the corporate laws in Delaware,
US.
The
material differences between the
Nova Scotia Companies Act
(the “NSCA”) as compared to the
Delaware General Corporation
Law
(“DGCL”) which may be of most interest to shareholders include the
following: (i) for material corporate transactions (such as amalgamations, other
extraordinary corporate transactions, amendments to the memorandum of
association and amendments to the articles of association) the NSCA generally
requires three-quarter majority vote by shareholders (and, in addition,
especially where the holders of a class of shares is being affected differently
from others, approval will be required by holders of two-thirds of the shares of
such class voting in a meeting called for the purpose), whereas DGCL generally
only requires a majority vote of shareholders for similar material corporate
transactions; (ii) quorum for shareholders meetings is not prescribed under the
NSCA and is only 5% under our articles of association, whereas under DGCL,
quorum requires the holders of a majority of the shares entitled to vote to be
present; and (iii) our articles of association require a special resolution and
the
Corporations Miscellaneous
Provisions Act
(Nova Scotia) requires three-quarters of all shareholders
entitled to vote to pass a resolution for one or more directors to be removed,
whereas DGCL only requires the affirmative vote of a majority of the
shareholders.
PROBABLE
ACQUISITIONS OR OTHER MATERIAL TRANSACTIONS
There are
no proposed undisclosed material transactions that have progressed to a state
where the Corporation believes that the likelihood of the Corporation completing
such a transaction is high. We continue to evaluate opportunities to amplify and
diversify our development portfolio through potential licensing,
acquisition or M&A activity.
USE
OF PROCEEDS
Unless
otherwise specified in a prospectus supplement, the net proceeds that we receive
from the issue of our securities will be used for working capital and general
corporate purposes. We intend to use the funds as stated in the applicable
prospectus supplement.
DESCRIPTION
OF SHARE CAPITAL, COMMON SHARES AND RELATED INFORMATION
Authorized
Capital
Our
authorized share capital consists of 500,000,000 common shares without nominal
or par value, 500,000,000 Class A non-voting common shares without nominal or
par value, 500,000,000 Class A preferred shares without nominal or par value and
500,000,000 Class B preferred shares, issuable in series, without nominal or par
value. As at September 16, 2009, there were 58,216,309 common shares, no Class A
non-voting common shares and no Class A or Class B preferred shares
outstanding.
The
following is a summary of the material provisions attached to the common shares,
the Class A preferred shares and the Class B preferred shares.
Common
Shares
All of
the common shares rank equally as to voting rights, participation in a
distribution of the assets of our corporation on a liquidation, dissolution or
winding-up of our corporation and the entitlement to dividends. The holders of
our common shares are entitled to receive notice of all meetings of shareholders
and to attend and vote the common shares at the meetings. Each common share
carries with it the right to one vote.
In the
event of the liquidation, dissolution or winding-up of our corporation, the
holders of our common shares will be entitled, subject to the rights,
privileges, restrictions and conditions attaching to any other class of shares
of our corporation, to receive, on a pro rata basis, share for share, with the
Class A non-voting common shares, all of the remaining property of our
corporation. There are no pre-emptive or conversion rights and no provisions for
redemption, retraction, purchase for cancellation or surrender or sinking or
purchase funds.
Class
A Preferred Shares and Class B Preferred Shares
There are
no Class A preferred shares or Class B preferred shares outstanding. The Class A
preferred shares and Class B preferred shares are issuable in series. Each
series may consist of such number of shares and have such designation, rights,
privileges, restrictions and conditions attached thereto as may be determined by
the board of directors, subject to the provisions attached to the Class A
preferred shares as a class or the Class B preferred shares as a class. The
Class A preferred shares and the Class B preferred shares each rank ahead of the
common shares with respect to the distribution of our assets upon liquidation,
dissolution or winding-up.
Shareholder
Rights Plan
On
November 28, 2007, our shareholders approved the renewal of a shareholder rights
plan. Pursuant to the renewed plan, the board of directors declared a
distribution of one right for each outstanding common share to shareholders of
record at the close of business on November 28, 2007 and authorized the issue of
one right for each common share issued after that date and before the date that
the plan expires or the rights separate from the common shares. The plan will
expire at the close of business at the annual meeting of our shareholders to be
held in 2017, subject to ratification of the plan by the shareholders every
three years. The rights will separate from the common shares at the close of
business on the eighth trading day (or such later day as determined by the board
of directors) after the public announcement of the acquisition of, or intention
to acquire, beneficial ownership of 20% or more of the common shares by any
person other than pursuant to a permitted bid. A “permitted bid” is an offer
that is made to the holders of all common shares (other than the offeror) in
compliance with the plan, is open for acceptance for at least 60 days, is
accepted by holders holding more than 50% of the common shares and, if so
accepted, is extended for a further 10 business days.
Dividend
Policy
We have
not paid any dividends since our incorporation. We will consider
paying dividends in future as our operational circumstances may permit having
regard to, among other things, our earnings, cash flow and financial
requirements. It is the current policy of the board of directors to
retain all earnings to finance our business plan.
Trading
Price and Volume
Our
common shares are listed on the TSX under the symbol “YM”, on the NYSE Amex
under the symbol “YMI” and on the AIM under the symbol “YMBA”. The following
table sets forth, for the periods indicated, the reported high and low prices
and the average volume of trading of the common shares on the TSX and the NYSE
Amex:
|
|
TSX (C$)
|
|
|
NYSE Amex (U.S.$)
|
|
Calendar Period
|
|
High
|
|
|
Low
|
|
|
Daily Avg.
Volume
|
|
|
High
|
|
|
Low
|
|
|
Daily Avg.
Volume
|
|
September
2008
|
|
|
0.65
|
|
|
|
0.42
|
|
|
|
28,596
|
|
|
|
0.63
|
|
|
|
0.41
|
|
|
|
119,458
|
|
October
2008
|
|
|
0.48
|
|
|
|
0.27
|
|
|
|
29,062
|
|
|
|
0.49
|
|
|
|
0.21
|
|
|
|
104,651
|
|
November
2008
|
|
|
0.58
|
|
|
|
0.33
|
|
|
|
39,933
|
|
|
|
0.54
|
|
|
|
0.25
|
|
|
|
161,220
|
|
December
2008
|
|
|
0.49
|
|
|
|
0.32
|
|
|
|
17,432
|
|
|
|
0.43
|
|
|
|
0.25
|
|
|
|
129,530
|
|
January
2009
|
|
|
0.49
|
|
|
|
0.40
|
|
|
|
32,219
|
|
|
|
0.43
|
|
|
|
0.32
|
|
|
|
83,471
|
|
February
2009
|
|
|
0.41
|
|
|
|
0.27
|
|
|
|
30,368
|
|
|
|
0.34
|
|
|
|
0.23
|
|
|
|
85,626
|
|
March
2009
|
|
|
0.48
|
|
|
|
0.29
|
|
|
|
56,631
|
|
|
|
0.40
|
|
|
|
0.20
|
|
|
|
126,584
|
|
April
2009
|
|
|
0.63
|
|
|
|
0.46
|
|
|
|
87,588
|
|
|
|
0.53
|
|
|
|
0.37
|
|
|
|
145,404
|
|
May
2009
|
|
|
0.63
|
|
|
|
0.48
|
|
|
|
71,383
|
|
|
|
0.60
|
|
|
|
0.42
|
|
|
|
290,780
|
|
June
2009
|
|
|
0.73
|
|
|
|
0.55
|
|
|
|
59,621
|
|
|
|
0.68
|
|
|
|
0.49
|
|
|
|
310,285
|
|
July
2009
|
|
|
0.75
|
|
|
|
0.55
|
|
|
|
28,234
|
|
|
|
0.70
|
|
|
|
0.48
|
|
|
|
162,070
|
|
August
2009
|
|
|
2.42
|
|
|
|
0.63
|
|
|
|
357,732
|
|
|
|
2.24
|
|
|
|
0.57
|
|
|
|
1,284,688
|
|
September
1, 2009 to September 15,
2009
|
|
|
1.99
|
|
|
|
1.51
|
|
|
|
136,841
|
|
|
|
1.82
|
|
|
|
1.40
|
|
|
|
674,055
|
|
DESCRIPTION
OF WARRANTS
We may
issue warrants to purchase common shares.
We will
not offer warrants for sale separately to any member of the public in the
Province of Ontario unless the offering is in conjunction with and forms part of
the consideration for an acquisition or merger transaction or unless the
prospectus supplement containing the specific terms of the warrants to be
offered separately is first approved for filing by the Ontario Securities
Commission.
The
prospectus supplement relating to any warrants offered hereunder will describe
the terms of the warrants and the applicable offering, including some or all of
the following:
·
|
the
designation and aggregate number of warrants
offered;
|
·
|
the
currency or currencies in which the warrants will be
offered;
|
·
|
the
number of common shares that may be purchased on the exercise of the
warrants and procedures that will result in an adjustment of that
number;
|
·
|
the
exercise price of the warrants;
|
·
|
the
dates or periods during which the warrants are
exercisable;
|
·
|
any
minimum or maximum amount of warrants that may be exercised at any one
time;
|
·
|
any
terms, procedures and limitations relating to the transferability,
exchange or exercise of the warrants;
and
|
·
|
any
other material terms of the
warrants.
|
Before
the exercise of their warrants, holders of warrants will not have any of the
rights of holders of common shares.
DESCRIPTION
OF UNITS
We may
issue units comprising any combination of the other securities described in this
prospectus. Each unit will be issued so that the holder of such unit
is also the holder of each security included in such unit. Therefore,
the holder of a unit will have the rights and obligations of a holder of each
included security (except in some cases where the right to transfer an included
security of a unit may not occur without the transfer of the other included
security comprising part of such unit).
The
prospectus supplement relating to any units offered hereunder will describe the
terms of the units and the applicable offering, including some or all of the
following:
·
|
the
designation and terms of the units and the securities comprising the
units, including whether and under what circumstances those securities may
be held or transferred separately;
|
·
|
any
provisions for the issuance, payment, settlement, transfer or exchange of
the units or of the securities comprising the
units;
|
·
|
whether
the units will be issued in fully registered or global
form.
|
The
preceding description and any description of units in the applicable prospectus
supplement do not purport to be complete and are subject to and are qualified in
their entirety by reference to the unit agreement, if any, and, if applicable,
collateral agreements relating to such units.
PLAN
OF DISTRIBUTION
We may
issue the securities offered by this prospectus in the Province of Ontario,
Canada, the United States and elsewhere where permitted by law for cash or other
consideration:
·
|
to
or through underwriters, dealers, placement agents or other
intermediaries,
|
·
|
directly
to one or more purchasers, or
|
·
|
in
connection with acquisitions by the
Corporation.
|
The
prospectus supplement with respect to the securities will set forth the terms of
the offering of the securities, including:
·
|
the
name or names of any underwriters, dealers or other placement
agents,
|
·
|
the
purchase price of, and form of consideration for, the securities and the
proceeds to us,
|
·
|
any
delayed delivery arrangements,
|
·
|
any
underwriting commissions, fees, discounts and other items constituting
underwriters’ compensation,
|
·
|
any
discounts or concessions allowed or reallowed or paid to dealers,
and
|
·
|
any
securities exchanges on which the securities may be
listed.
|
Only the
underwriters named in a prospectus supplement are deemed to be underwriters in
connection with the securities offered by that prospectus
supplement.
The
securities may be sold, from time to time in one or more transactions at a fixed
price or prices which may be changed or at market prices prevailing at the time
of sale, at prices related to such prevailing market price or at negotiated
prices.
Under
agreements which may be entered into by us, underwriters, dealers and agents who
participate in the distribution of securities may be entitled to indemnification
by us against certain liabilities, including liabilities under the United States
Securities Act of 1933
,
as amended, and applicable Canadian provincial securities legislation, or to
contribution with respect to payments which such underwriters, dealers or agents
may be required to make in respect thereof. The underwriters, dealers and agents
with whom we enter into agreements maybe customers of, engage in transactions
with, or perform services for, us in the ordinary course of
business.
In
connection with any offering of securities, the underwriters may over-allot or
effect transactions which stabilize or maintain the market price of the
securities offered at a level above that which might otherwise prevail in the
open market. Such transactions, if commenced, may be discontinued at any
time.
CERTAIN
INCOME TAX CONSIDERATIONS
The
applicable prospectus supplement may describe the principal Canadian federal
income tax considerations generally applicable to investors described therein of
purchasing, holding and disposing of securities, including, in the case of an
investor who is not a resident of Canada, Canadian non-resident withholding tax
considerations.
The
applicable prospectus supplement may also describe certain United States federal
income tax consequences of the acquisition, ownership and disposition of any
securities offered under this prospectus by an investor who is a United States
person (within the meaning of the United States Internal Revenue
Code).
AUDITORS
The
consolidated financial statements as at June 30, 2008 and 2007 and for each of
the years in the three year period ended June 30, 2008 incorporated in this
prospectus by reference have been audited by KPMG LLP, independent registered
chartered accountants, as stated in their report, which is incorporated herein
by reference.
LEGAL
MATTERS
Certain
legal matters relating to the securities offered by this prospectus will be
passed upon for us by Heenan Blaikie LLP, Toronto, Ontario, with respect to
matters of Canadian law, and Dorsey & Whitney LLP, Vancouver, B.C. and New
York, NY with respect to matters of United States law. The partners
and associates of Heenan Blaikie LLP and Dorsey & Whitney LLP beneficially
own, directly or indirectly, less than 1% of any class of securities issued by
YM.
TRANSFER
AGENT AND REGISTRAR
The
transfer agent and registrar for the common shares is CIBC Mellon Trust Company
at its principal office in Toronto, Ontario.
DOCUMENTS
FILED AS PART OF THE REGISTRATION STATEMENT
The
following documents have been filed or will be filed with the SEC as part of the
registration statement of which this prospectus forms a part: the documents
listed under “Documents Incorporated by Reference”; consents of accountants and
counsel; and powers of attorney.
YM Biosciences (AMEX:YMI)
過去 株価チャート
から 6 2024 まで 7 2024
YM Biosciences (AMEX:YMI)
過去 株価チャート
から 7 2023 まで 7 2024